Fluorine containing vinyl ethers

Field:

The present invention relates to perfluorinated vinyl ethers as valuable comonomers for fluoroelastomers with enhanced low temperature properties.

Background:

The benefits of modifying fluoropolymers by vinyl ethers are described in various review articles. See, for example, <nplcit id="ncit0001" npl-type="b"><text>Modem Fluoropolymers, John Scheirs, Wiley Series in Polymer Science 1997 </text></nplcit>and in other literature (e.g. <nplcit id="ncit0002" npl-type="s"><text>Emel 'yanov et al, Zh. Org. Khim (1994) 30(8) 1266-70</text></nplcit>; <patcit id="pcit0001" dnum="US4273728A"><text>Krespan, Carl G., DuPont de Nemours U. S. 4,273,728</text></patcit>).

Partly fluorinated vinyl ethers and their copolymers are described in A. E. Feiring et al, <patcit id="pcit0002" dnum="US5326917A"><text>DuPont de Nemours U.S. 5,326,917</text></patcit>. Long chain vinyl ethers provide in fluoroelastomers excellent low temperature properties (see <patcit id="pcit0003" dnum="US4513128A"><text>Uschold et al, U.S. Patent 4,513,128</text></patcit>).

The preparation of perfluoro(alkyl vinyl ethers) by fluorination with elemental fluorine is known. See <patcit id="pcit0004" dnum="US5350497A"><text>Hung et al, U.S. Patent 5,350,497</text></patcit>. This patent discloses the fluorination of selected partially fluorinated (di)chloroethyl ethers (followed by dehalogenation to the corresponding perfluoro(alkyl vinyl ether).

Perfluorinated long chain perfluoroethers are difficult to prepare, especially those vinyl ethers without branching and more than 3 atoms in the alkyl group. For example, perfluorovinyl ethers are commonly prepared by two routes. See, for example, <nplcit id="ncit0003" npl-type="b"><text>Modem Fluoropolymers, J. Scheirs, Wiley 1997 pp 376-378</text></nplcit>. <chemistry id="chem0001" num="0001"><img file="EP1240125B2_D0001.tif" /></chemistry> Addition of perfluorinated acid fluorides to hexafluoropropylene oxide results in an acid fluoride that may be converted to a salt and pyrolyzed to give the described perfluorovinyl ether. The oligomerization of hexafluoropropylene oxide with itself and conversion to a salt and subsequent pyrolysis gives long chain but branched ethers. <chemistry id="chem0002" num="0002"><img file="EP1240125B2_D0002.tif" /></chemistry> A more recent process prepares perfluorovinyl ethers by using perfluoro alkyl hypofluorites and dichlorodifluoroethylene followed by dehalogenation using, for example, Zn. <chemistry id="chem0003" num="0003"><img file="EP1240125B2_D0003.tif" /></chemistry> As noted, it is difficult to provide long chain perfluorinated ethers, especially vinyl ethers, when using these processes. A difficulty in the dichloro process includes the hazards of making and handling the R²+OF species. Because of these hazards, this species also has a limited avaitability. An improved process for making perfluorinated vinyl ethers is needed, particularly for making linear perfluorinated vinyl ethers.

Summary:

The present invention also relates to a fluoroelastomer as defined in the claim.

As used herein, the term perfluorinated means that all of the carbon bonded hydrogen atoms have been replaced with fluorine and any unsaturated carbon-carbon bonds have been saturated with fluorine In the following methods of making vinylether are described that include vinylethers as recited in the claim. The methods and the vinyl ethers obtained are not claimed.

In a first embodiment of the process suitable for making perfluorinated vinylethers like the ones as claimed, an appropriate hydrocarbon (e.g., containing at least one 2-alkoxy propionate moiety, derivative or equivalent) precursor is provided which includes a hydro- carbon acid derivative. Such derivatives include, for example, acid fluorides, anhydrides, esters and the like. This derivative is then perfluorinated to provide a corresponding perfluorinated acid derivative intermediate. The intermediate is then converted to its corresponding perfluorinated acid metal salt and subsequently converted to the desired perfluorovinyl ether.

In a second embodiment of a process suitable for making perfluorinated vinylethers like the ones claimed, a partially fluorinated hydrocarbon precursor is provided by reacting hexafluoropropylene oxide with an alcohol or a species such as sodium alkoxide. The precursor is then fully fluorinated by replacing any remaining carbon bonded hydrogen atoms with fluorine atoms to provide a perfluorinated acid derivative intermediate. The intermediate is then converted to its corresponding per- fluorinated metal salt and subsequently converted to the desired perfluorovinyl ether.

In a third embodiment for a process suitable for making perfluorinated vinylethers like the ones claimed, a partially fluorinated hydrocarbon precursor is provided by reacting a fluorinated olefin with an alcohol, 2) fully fluorinating the precursor, 3) hydrolyzing the fluorinated precursor to an acid derivative, 4) converting the acid derivative to its corresponding perfluorinated acid metal salt, 5) converting the salt product to its corresponding perfluorovinyl ether.

In the claimed invention a perfluorovinyl ether having the formula R_fOCF₂OCF=CF₂ is used as comonomer wherein R_f is as recited in the claim.

Detailed Description:

The perfluorinated vinyl ethers recited in the claim are useful in the preparation of fluoroelastomers, especially those that are used at low temperatures. Similar elastomers are known. See, for example, <patcit id="pcit0005" dnum="US4513128A"><text>Uschold et al., U.S. Patent 4,513,128</text></patcit>.

The embodiment of the process suitable for making the perfluorinated vinyl ethers like the ones as claimed selectedis not critical to the practice of the invention. However, there are certain process steps common to each of the embodiments. The process and the perflorinated vinyl ethers obtained by it are not claimed.

Fluorination of the precursors may be accomplished by either electrochemical fluorination (ECF) or direct fluorination (DF). ECF is described in <patcit id="pcit0006" dnum="US2713593A"><text>U.S. Patent 2,713,593</text></patcit> and <patcit id="pcit0007" dnum="WO9850603A"><text>WO 98/50603</text></patcit>. DF is described in <patcit id="pcit0008" dnum="US5488142A"><text>U.S. Patent 5,488,142</text></patcit>.

Conversion of the perfluorinated precursor to the metal salt is preferably accomplished by treatment with a base, e.g. saponification.

Conversion of the perfluorinated metal salt to the vinyl ether is preferably accomplished by pyrolysis. Typically this is done by drying the salt and then heating the salt to a temperature of from 170° C to 250° C with or without the presence of a solvent or other medium.

The following discussion specifically addresses three embodiments of the process suitable for making the perfluorinated vinyl ethers like the ones recited in the claim. It is not intended to limit the scope of the disclosure to these embodiments. Rather it illustrates the versatility of the process, however, the process and the vinyl ether obtained by it are not claimed.

In the first embodiment of a process suitable for making a perfluorinated vinlyether like the ones recited in the claim, the perfluorovinyl ether may be prepared by <ol id="ol0001" compact="compact" ol-style=""><li>(a) providing a hydrocarbon ester, anhydride, acid halide or acid precursor which comprises at least one 2-alkoxypropionate moiety, derivative or equivalent,</li><li>(b) fluorinating the precursor to provide a perfluorinated acid derivative intermediate,</li><li>(c) converting the perfluorinated intermediate to its perfluorinated metal salt, and</li><li>(d) pyrolyzing the perfluorinated metal salt to the corresponding perfluorovinyl ether.</li></ol> More specifically, the first embodiment may be exemplified by the following synthesis sequence: <maths id="math0001" num=""><math display="block"><mrow><msub><mi mathvariant="normal">R</mi><mi mathvariant="normal">b</mi></msub><mi mathvariant="normal">OCH</mi><mfenced><msub><mi mathvariant="normal">CH</mi><mn mathvariant="normal">3</mn></msub></mfenced><mi mathvariant="normal">C</mi><mfenced><mi mathvariant="normal">O</mi></mfenced><msub><mi mathvariant="normal">X</mi><mi mathvariant="normal">b</mi></msub><mover><mrow><mo>→</mo></mrow><mrow><mspace width="2em" /><msub><mi mathvariant="normal">F</mi><mn mathvariant="normal">2</mn></msub><mspace width="1em" /></mrow></mover><msub><mi mathvariant="normal">R</mi><mi mathvariant="normal">f</mi></msub><mi mathvariant="normal">OCF</mi><mfenced><msub><mi mathvariant="normal">CF</mi><mn mathvariant="normal">3</mn></msub></mfenced><mi mathvariant="normal">C</mi><mfenced><mi mathvariant="normal">O</mi></mfenced><msub><mi mathvariant="normal">X</mi><mi mathvariant="normal">f</mi></msub><munderover><mrow><mo>→</mo></mrow><mrow><mspace width="1em" /><mn mathvariant="normal">2.</mn><mi mathvariant="normal">Heat</mi><mspace width="1em" /></mrow><mrow><mn mathvariant="normal">1.</mn><mi mathvariant="normal">Base</mi></mrow></munderover></mrow></math><img file="EP1240125B2_D0004.tif" /></maths>         R_fO-CF=CF₂ where R_h is a C₁-C₂₀ alkyl or aromatic group, which may be linear, branched, cyclic and which may contain additional ether linkages. The X_h moiety is selected from the group consisting of P_h, lower alkoxy, (such as -OCH₃, -OCH₂CH₃), OC(O)CH(CH₃)OR_h, -F and -Cl. R_f is a perauorinated version of R_h and X_f is a perfluorinated version of X_h.

In the case where a divinyl ether is desired, a precursor may be represented as         R'_h(OCH(CH₃)C(O)X_h)₂ where R'_h is described in a similar manner to R_h above except it is divalent. The R_h moieties in this particular precursor may be the same or different. Such a divinyl ether is CF₂=CFOR'_fOCF=CF₂ wherein R'_f is a perfluorinated version of R'_h.

In an additional possibility, the pendant methyl group of the -CH(CH₃)COO- moiety may contain a chlorine atom. This chlorine atom will survive the fluorination step and may provide some reactive advantage in subsequent steps.

When R₁ is linear, this route opens new possibilities for the synthesis of long chain, non-branched vinyl ether in an efficient and economical way and is not limited to certain sequences in the side chain. In contrast see, for example, Masahiro et al, <patcit id="pcit0009" dnum="EP290848A"><text>Daikin EP 290,848</text></patcit> where the molecule is limited to a repetition of the sequence (-OCF₂CF₂CF₂-).

An alternate approach to the hydrocarbon precursor for this embodiment involves esters of 2-alkoxy-1-propanol. This precursor has the configuration of the ester moiety reversed when compared to the first reaction sequence listed, but is functionally equivalent to a 2-alkoxypropionate in the process of this invention. The precursor is then perfluorinated as described above. The resulting species then is dissociated to produce the perfluoro-2-alkoxy propionyl fluoride. From this point the conversion to the vinyl ether proceeds as in the first reaction sequence by converting the propionyl fluoride to the corresponding perfluorinated metal salt and pyrolyzing the salt to the corresponding perfluorovinyl ether.

An additional precursor which may be used in this route includes         R³OCH(CH₂Cl)CH₂OA_c where R³ is an alkyl group which may contain additional ether linkages and <chemistry id="chem0004" num="0004"><img file="EP1240125B2_D0005.tif" /></chemistry> or with the alkyl being a C₁-C₆ alkyl group. Preferably, the alkyl is a C₁ alkyl group that may be fluorinated. The chlorine on the pendent methyl group will also survive the fluorination process.

The hydrocarbon containing precursors are either commercially available or are easily prepared by common organic synthesis. Corresponding long chain polyether alcohols may be coupled with 2-chloropropionic acid to achieve the desired precursors, but any other method is also useful. Examples of ester precursors for fluorination include the following precursors and reference (*) precursors:         CH₃OCH(CH₃)COOCH₃ (*)         [CH₃OCH(CH₃)CO]₂O (*)         CH₃OCH(CH₃)CH₂OCOCH₃ (*)         CH₃OCH(CH₃)CH₂OCOCF₃ (*)         CH₃OCH(CH₃)CH₂OSO₂CF₃ (*)         CH₃OCF(CF₃)COOCH₃ (*)         [CH₃OCF(CF₃)CO]₂O (*)         CHF₂OCH(CH₃)COOCH₃ (*)         CH₃OCH(CH₂Cl)COOCH₃ (*)         HCF₂CF₂OCH(CH₃)COOCH₃ (*)         CF₃CH₂OCH(CH₃)COOCH₃ (*)         CH₃OCH₂OCH(CH₃)COOCH₃         C₂H₅OCH₂OCH(CH₂Cl₂)CH₂OCOCH₃         CH₃OCH₂CH₂OCH(CH₃)COOCH₃ (*)         CH₃OCH₂CH₂ CH₂OCH(CH₃)COOCH₃ (*)         CH₃OCH(CH₃)CH₂CH₂OCH(CH₃)COOCH₃ (*)         C₂H₅OCH₂CH₂CH₂CH₂OCH(CH₃)COOCH₃ (*)         CF₃OCF₂CHFCF₂OCH(CH₃)COOCH₃ (*)         CF₃OCHFCF₂OCH(CH₃)COOCH₃ (*)         CF₃CHFCF₂OCH(CH₃)COOCH₃ (*)         C₂H₅OC₂H₄OC₂H₄OCH(CH₃)COOCH₃ (*)         nC₃F₇CH₂OCF(CF₃)COCl (*)         nC₃F₇CH₂OCF(CF₃)COF (*)         (CH₃)₂CHCH₂OCH(CH₃)COOCH₃ (*)         C₈H₁₇OCH(CH₃)COOCH₃ (*)         C₈F₁₇C₂H₄OCH(CH₃)COOCH₃ (*)         C₆H₅OCH(CH₃)COOCH₃ (*)         4-CH₃OC₆H₄OCH(CH₃)COOCH₃ (*)         CF₃OCFHCF₂OCH₂OCH(CH₃)CO₂CH₃

Fluorination of the precursors can be done by electrochemical fluorination (ECF) as previously described. ECF may be operationally simpler because only one reactor is used. However, ECF tends to give lower yields of some species because of C-O and C-C bond cleavage reactions.

In contrast, direct fluorination (OF) conducted according to <patcit id="pcit0010" dnum="US5476974A"><text>U.S. Patent Nos. 5,476,974</text></patcit> or <patcit id="pcit0011" dnum="US5488142A"><text>5,488, 142</text></patcit> leads to little or no rearrangement and only minor losses attributable to cleavage reactions. Thus, in spite of the need for both a fluorine generator and a direct fluorination reactor, OF is preferred in most cases because of a higher yield of the desired product.

Some partially fluorinated precursors, such as 2,3,3,3-tetrafluoropropionic derivatives of the second embodiment give little rearrangement and less cleavage in ECF than the unfluorinated precursors.

The resulting perfluorinated esters, anhydrides or acid fluoride end groups may be converted to the corresponding hydrocarbon methyl esters with methanol if a separation step (e.g. distillation) is desired to purify the reaction product. This is typically done to separate the perfluorinated compounds from the reaction media. Either the separated product or the perfluorinated products in the reaction mixture are then saponified with bases, i.e. converted to a salt, (e.g. KOH, Na₂CO₃, NaOH) to give the resulting salts. The salts are then dried and pyrolyzed at temperatures from 170°C to 250°C with or without solvent to give the corresponding perfluorovinyl ether. The resulting perfluorovinyl ether is preferably purified by distillation to obtain the desired purity.

In a second embodiment of the process suitable for use in the invention a partially fluorinated hydrocarbon precursor is used. This precursor is prepared by reacting hexafluoropropylene oxide with an alcohol (such as is described in <nplcit id="ncit0004" npl-type="s"><text>D. Sianesi et al., J. Org. Chem., Vol. 3 (1966), p. 2312</text></nplcit>). This process comprises the steps of: <ol id="ol0002" compact="compact" ol-style=""><li>(a) providing a partially fluorinated hydrocarbon precursor by reacting hexafluoropropylene oxide with an alcohol,</li><li>(b) perfluorinating the precursor, for example, by electrochemical or direct fluorination, to provide a perfluorinated ester or acid intermediate,</li><li>(c) converting the perfluorinated intermediate to its corresponding metal salt, and</li><li>(d) pyrolyzing the perfluorinated salt at a temperature sufficient to provide a perfluorovinyl ether.</li></ol> This process is represented by the following synthesis sequences. <chemistry id="chem0005" num="0005"><img file="EP1240125B2_D0006.tif" /></chemistry> R_fO-CF=CF₂ , wherein R_f and R_h are as described above.

The fluorination, conversion to a salt and pyrolysis to the perfluorovinyl ether are done in a manner similar to that described in the first embodiment.

In a third embodiment of the process suitable for making perfluorinated vinyl ethers like the ones recited in the claim, a perfluorinated vinyl ether may be prepared by a process comprising the steps of: <ol id="ol0003" compact="compact" ol-style=""><li>(a) providing a partially fluorinated precursor which is a reaction product of a fluorinated olefin and an ester of lactic acid,</li><li>(b) perfluorinating the precursor, to provide a corresponding perfluorinated ester or acid derivative intermediate,</li><li>(c) converting the perfluorinated intermediate to its corresponding metal salt, and</li><li>(d) pyrolyzing the perfluorinated salt to the corresponding perfluorovinyl ether.</li></ol>

More specifically, the third embodiment of the process is exemplified by the following synthesis sequences. <chemistry id="chem0006" num="0006"><img file="EP1240125B2_D0007.tif" /></chemistry> where n = 0 or 1, and R"r is F or R_f when n is 0, and R"_f is R_f when n is 1, and R' is an C1 to C6 alkyl.

Preferred olefins for the addition to the hydrocarbon ester are tetrafluoroethylene, hexafluoropropene, perfluoro(alkyl vinyl) ethers, such as perfluoro(methyl vinyl) ether, perfluoro(propyl vinyl) ether or other perfluoro vinyl ethers as described herein. The preferred bases to catalyze the addition are alkali hydroxides KOH, NaOH, or NaOMe. Solvents for the reaction include N,N-dialkyl carboxylic acid amides, such as those disclosed in <patcit id="pcit0012" dnum="US4433180A"><text>U.S. Patent No. 4,433,180</text></patcit> (von Wemer). The 2-alkoxy propionate moiety is supplied by the hydrocarbon ester in this embodiment.

The resulting partially fluorinated precursors are fluorinated to provide a perfluorinated acid derivative intermediate. This step may be accomplished by either ECF or DF as discussed above. The solvents for the direct fiuorination embodiments are perfluorinated compounds and/or fluorochloro compounds, e.g. perfluoromethylmorpholine, Freon-113, etc.

The perfluorinated intermediate is then converted to a metal salt. The salt is then pyrolyzed to the corresponding perfluorovinyl ether. These steps are accomplished in a manner similar to that described in the first embodiment.

Examples of perfluorinated vinyl ethers made according to one or more of the methods described above include the following compounds and reference (*) compounds         CF₃O(CF₂)₃OCF=CF₂ (*) and         R_f-OCF₂OCF=CF₂, including         CF₃OCF₂OCF=CF₂ and         C₂F₅OCF₂OCF=CF₂

Examples:

Reference Example 1 - Perfluoro (methoxyethyl) vinyl ether (not claimed)

Methyl 2-(methoxyethoxy) propionate was prepared by the alkylation of methoxyethanol (1500g, 19.7m) with 2-chloropropionic acid (1050g, 9.7m), using NaOH (790g, 19.?m) and tetrabutylammonium bromide (40g, 0.12m) in 1.2 liters of THF. After removal of the excess starting alcohol, methanol (965g, 30m) and HCl (382g, 10.5m) were added. Distillation gave the desired ester (832g, 5.1m, 53% yield) b.p: 100-120°C/15mm (2.0 kPa) identified by H-nmr. The ester was fluorinated in perfluoro-N-methylmorpholine (PMM) as described in <patcit id="pcit0013" dnum="US5488142A"><text>U.S. Patent 5,488,142</text></patcit>. After fluorination, methanol (850g, 26.6m) was added and distillation gave methyl perfluoro 2-(methoxyethoxy) propionate (1334g, 3.7m, 56% yield) b. p. rn-115°C, identified by 19F NMR. The fluorinated ester (500g,1.39m) was reacted with KOH (93g,1.4m) dissolved in 400g of methanol to give the corresponding salt. The salt was stripped of methanol and water at 90°C/15mm (2.0 kPa) after the addition of 21 g K₂CO₃ and 1000g of Fluorinert™ FC71 (from 3M Co.). Vacuum was broken and the salt decarboxylated at 180-220°C. Perfluoro (methoxyethyl) vinyl ether was distilled (299g, 1.06m, 76% yield) b. p. 46-48°C, identified by 19F NMR.

Table 1 lists perfluorovinyl ethers prepared in a manner similar to Reference Example 1 using the listed starting material. The boiling points (bp) listed were measured at atmospheric pressure. <tables id="tabl0001" num="0001"><table frame="none"><title><b>TABLE 1</b></title><tgroup cols="4" colsep="0" rowsep="0"><colspec colnum="1" colname="col1" colwidth="17mm" /><colspec colnum="2" colname="col2" colwidth="56mm" /><colspec colnum="3" colname="col3" colwidth="41mm" /><colspec colnum="4" colname="col4" colwidth="13mm" /><thead><row><entry valign="top"><b>Ref.Ex.</b></entry><entry valign="top"><b>Starting Material</b></entry><entry valign="top"><b>Product</b></entry><entry valign="top"><b>Bp</b></entry></row></thead><tbody><row><entry>1</entry><entry><chemistry id="chem0007" num="0007"><img file="EP1240125B2_D0008.tif" /></chemistry></entry><entry>CF₃-O-(CF₂)₂-O-CF=CF₂</entry><entry>48°C</entry></row><row><entry>2</entry><entry><chemistry id="chem0008" num="0008"><img file="EP1240125B2_D0009.tif" /></chemistry></entry><entry>C₃F₇-O-CF=CF₂</entry><entry>39°C</entry></row><row><entry>3</entry><entry><chemistry id="chem0009" num="0009"><img file="EP1240125B2_D0010.tif" /></chemistry></entry><entry>CF₃-O-(CF₂)₃-O-CF=CF₂</entry><entry>64°C</entry></row></tbody></tgroup></table></tables>

Reference Example 4 - Perfluoro(methyl vinyl) ether (not claimed)

Hexafluoropropylene oxide was reacted with methanol at room temperature to give in almost quantitative yield CH₃-O-CF(CF₃)-COOCH₃ This product was then fluorinated in perfluoro(methyl morpholine) in a tubular reactor as described in <patcit id="pcit0014" dnum="US5488142A"><text>U. S. Patent 5,488,142</text></patcit>. The resulting perfluorinated compound was isolated and saponified with potassium hydroxide. The resulting salt was dried and pyrolyzed at 250°C to give perfluoromethylvinyl ether in a 60% molar yield.

Table 2 lists vinyl ethers produced in a manner similar to Reference Example 4, but using the listed starting alcohol. Boiling points were measured at atmospheric pressure. <tables id="tabl0002" num="0002"><table frame="all"><title>TABLE2</title><tgroup cols="4"><colspec colnum="1" colname="col1" colwidth="17mm" /><colspec colnum="2" colname="col2" colwidth="31mm" /><colspec colnum="3" colname="col3" colwidth="44mm" /><colspec colnum="4" colname="col4" colwidth="13mm" /><thead><row><entry align="center" valign="top"><b>Ref. Ex.</b></entry><entry valign="top"><b>Starting Alcohol</b></entry><entry valign="top"><b>Product</b></entry><entry valign="top"><b>Bp</b></entry></row></thead><tbody><row rowsep="0"><entry align="center">4</entry><entry>CH₃OH</entry><entry>CF₃-O-CF=CF₂</entry><entry>-</entry></row><row rowsep="0"><entry align="center" /><entry /><entry /><entry>23°C</entry></row><row rowsep="0"><entry align="center">5</entry><entry>C₃H₇OH</entry><entry>C₃F₇-O-CF=CF₂</entry><entry>36°C</entry></row><row><entry align="center">6</entry><entry>CH₃OCH₂CH₂OH</entry><entry>CF₃-O-CF₂-CF₂-O-CF=CF₂</entry><entry>48°C</entry></row></tbody></tgroup></table></tables>

Reference Example 7. Perfluoro octyl vinyl ether (not claimed)

In a procedure similar to Reference Example 1, 1-octanol was converted to methyl 2-octyloxypropionate, bp 100-110C/10mm (1.3 kPa), and 764.5 g (3.54 mol) of this was fluorinated in a 20 liter reactor according to the procedure of <patcit id="pcit0015" dnum="US5476974A"><text>U.S. Patent 5,476,974</text></patcit> in CF₂ClCFCl₂ solvent. Methanolysis and distillation gave 1143g (54%) C₈ F₁₇OCF(CF₃) COOMe, and saponification and pyrolysis gave C₈F₁₇OCF=CF₂, bp 136-137°C.

Reference Example 8. Perfluoro 3-methoxypropyl vinyl ether, CF

3

O(CF

2

)

3

OCF=CF

2

(not claimed)

In a procedure similar to Reference Example 1, CH₃O(CF₂)₃OH was converted to CF₃O(CF₂)₃OCF(CF₃) COOMe bp 123-126°C and this to CF₃O(CF₂)₃OCF=CF₂ bp 62-64°C.

Reference Example 9. Perfluoro 3-methoxybutyl vinyl ether, CF

3

OCF(CF

3

)C

2

F

4

OCF=CF

2

(not claimed)

In a procedure similar to Reference Example 1, CH₃OCH(CH₃)C₂ H₄OH was converted to CF₃OCF(CF₃) C₂F₄OCF(CF₃)COOMe bp 145-148°C and this to CF₃OCF(CF₃)C₂F₄OCF=CF₂, bp 84-86°C.

Reference Example 10. Perfluoro 2,6-dimethylcyclohexyl vinyl ether (not claimed)

In a procedure similar to Reference Example 1, 2,6-dimeihylphenol was converted to 2,6-(CF₃)₂-cyclic-C₆F₉OCF(CF₃)COOMe, bp 75-80°C/3mm (0.4 kPa), and this was then converted to 2,6-(CF₃)₂-cyclic-C₆F₉OCF=CF₂ bp136-138° C.

Reference Example 11. Perfluoro ethoxyethoxyethyl vinyl ether CF

3

CF

2

OC

2

F

4

OC

2

F

4

OCF=CF

2

(not claimed)

In a procedure similar to Reference Example 1, ethoxyethoxyethanol was converted to CF₃CF₂OC₂F₄OC₂ F₄OCF(CF₃)COOMe, bp 170-175°C, and this to CF₃CF₂OC₂ F₄OC₂ F₄OCF=CF₂, bp 92-95°C.

Reference Example 12. Perfluoro propyl vinyl ether, C

3

F

7

OCF=CF

2

(not claimed)

In a procedure similar to Reference Example 1, n-propanol was converted to 2-propoxypropionic acid. This upon treatment with acetyl chloride afforded the anhydride (C₃H₇OCH(CH₃)CO)₂O, bp 118-22°C/15 mm (2.0 kPa), which upon direct fluorination according to <patcit id="pcit0016" dnum="US5488142A"><text>U.S. Patent 5,488,142</text></patcit> gave (C₃F₇OCF(CF₃) CO)₂O, bp 186-190°C. The perfluoroanhydride was methanolysed to C₃F₇OCF(CF₃)COOMe, bp 118-122°C and converted to C₃F₇OCF=CF₂, bp 36°C.

Reference Example 13. Perfluoro methyl vinyl ether, CF

3

OCF=CF

2

(not claimed)

In a procedure similar to Reference Example 12, 2-methoxypropionic acid was converted to the anhydride (CF₃OCF(CF₃)CO)₂O. This was methanolysed to CF₃OCF(CF₃)COOMe bp 58-62°C and this converted to CF₃OCF=CF₂ bp -23°C.

Reference Example 14. Perfluoro methyl vinyl ether from 2-methoxy-1-propyl acetate (not claimed)

NaH (60% in mineral oil, 8.0g, 0.2 mol) was washed with hexane, slurried in THF, and treated dropwise with 26.4g (0.2 mol) 1-t-butoxy-2-propanol (Aldrich Chemical) with ice cooling. The mixture was stirred at reflux one hr, chilled in ice, and treated with 19 ml (0.2 mol) dimethyl sulfate. After heating at reflux for 3 hr, the mixture was filtered, concentrated, and distilled to a head temperature of 85°C. The residue (23.9g yellow liquid) was &gt;90% pure 1-t-butoxy-2-methoxypropane by 1H NMR analysis. Of this, 10.0g was mixed with 0.05g fused zinc chloride and 15 ml dichloromethane, chilled in ice, and treated slowly with 6.0g acetyl chloride. On warming to room temperature, gas evolution was noted. The mixture was distilled to 8.0g at about 50°C/14 Torr. 1H NMR and gc/ms confirmed 2-methoxy-1-propyl acetate in &gt;90% purity, the main impurity being the product derived from the minor regioisomer 2-t-butoxy-1-propanol (present at about 7% in the starting material). This ester was direct fluorinated as described in <patcit id="pcit0017" dnum="US5488142A"><text>U.S. Patent 5,488, 142</text></patcit>. The resulting solution was analyzed by ¹⁹F NMR to contain CF₃OCF(CF₃)CF₂OCOCF₃ in 43% yield. Methanalysis gave the same methyl ester as Reference Example 13. One could then convert to the perfluorovinyl ether as described above.

Reference Example 15. Perfluoro methyl vinyl ether from methyl 2-methoxypropionate (not claimed)

Methyl 2-methoxypropionate (520.3g) was fluorinated in an ECF cell as described in <patcit id="pcit0018" dnum="US2713593A"><text>U.S. Patent 2,713,593</text></patcit> equipped with -40°C and -80°C condensers. The yield of CF₃OCF(CF₃)COF was estimated as 17%. One could then convert this to perfluoromethylvinyl ether as described above.

Example 1. Perfluoro ethoxymethyl vinyl ether, C

2

F

5

OCF

2

OCF=CF

2

(not claimed)

Ethyl 2-ethoxymethoxypropionate was made by stirring and heating a mixture of 1007g (8.5 mol) ethyl lactate, 2500 ml (20.2 mol) diethoxymethane (DEM), and 5.0g toluenesulfonic acid hydrate under nitrogen while distilling off a mixture of ethanol and DEM. Fresh DEM was periodically added. After 12 hr, the mixture was cooled, washed with very dilute NaOH, and the product distilled to 1232g (7.5 mol, 88%) bp 90°C/20 mm (2.7 kPa). This ester was direct fluorinated as described in <patcit id="pcit0019" dnum="US5488142A"><text>U.S. Patent 5,488, 142</text></patcit> and the product treated with methanol to give C₂ F₅OCF₂OCF(CF₃) COOMe bp 107-112°C in 30% yield. A crude sample (2342g, 57% assay, remainder PMM and CF₃COOMe) was added to a stirred solution of 300g NaOH in 800g water at about 30°C. After stirring 18 hr, the mixture was treated with 1 liter 50% sulfuric acid and the lower phase distilled to 718g bp 60°C/l mm (0.13 kPa) as the carboxylic acid. A second batch of 2406g crude ester yielded 896g, and rewashing of the combined distillation residues with 50% sulfuric acid yield an additional 412g, for a total yield of 2029g of the carboxylic acid. Of this 1000g was mixed with 500g powdered sodium carbonate in 2.5 l. acetone for 24 hr, filtered and stripped to give C₂ F₅OCF₂OCF(CF₃)COONa, a tan solid. A solution of 365.8g in 200 ml diethyl ether was mixed with 250 ml Fluorinert FC-71 (3M Co.), stripped at 20 mm (2.7 kPa) for 20 min, and heated to 224°C, at which time volatile product began collecting in the dry-ice cooled traps. Heating was continued for 3 hr, final temperature was 245°C. The product, the corresponding perfluorovinyl ether with a bp of 46°C, was recovered by fractionation.

Example 2. Perfluoro ethoxymethyl vinyl ether from 3-chloro-2-(ethoxymethoxy)-1-propyl acetate (not claimed)

A mixture of 10.0g FeCl₃ and 276 ml acetic acid was treated slowly with 312 ml epichlorohydrin at 5 to 15°C (dry-ice bath). The product was mixed with 5.1g NaOAc and filtered to 497.1 g amber liquid, a 87-13 mixture of HOCH (CH₂Cl)CH₂OAc and AcOCH(CH₂Cl)CH₂OH. A solution of 304g of the above mixture and 200g ClCH₂OEt in 600 ml methylene chloride was chilled in ice while adding 260 N,N-diisopropyl ethylamine. Distillation yielded 257.0g bp 80°C/ 1.2mm (0.17 kPa). The major components were identified by gc/ms, ¹H-NMR, and ¹³C-NMR as C₂H₅OCH₂OCH (CH₂Cl)CH₂OAc (65%), AcOCH(CH₂Cl)CH₂OCH₂OC₂H₅ (18%) and starting alcohols (13%). Fluorination according to <patcit id="pcit0020" dnum="US5488142A"><text>U.S. Patent 5,488,142</text></patcit> and distillation of the PMM solvent left 184.1g perfluorinated ester as residue. This was treated with about 0.5 ml pyridine, according to <patcit id="pcit0021" dnum="US5466877A"><text>U.S. Patent 5,46-6,877</text></patcit>, with vigorous outgassing and formation of C₂F₅OCF₂OCF(CF₂Cl)COF, distilled to 90.2g bp 85-95°C. ¹⁹F-NMR shows this to be 73% pure. One could then convert this to the perfluorovinyl ether as described for other 3-chloro-perfluoro-(2-alkoxypropionates) in <patcit id="pcit0022" dnum="US5449825A"><text>U.S. Patent 5,449,825</text></patcit>.

Reference Example 16. Perfluoro methyl vinyl ether (not claimed)

Hexafluoropropylene oxide (HFPO, 300g) was added to 50g of 25% sodium methoxide in methanol plus 450g methanol at room temperature in a modification of the procedure of (<nplcit id="ncit0005" npl-type="s"><text>J. Org. Chem. 31, 2312 (1960</text></nplcit>) to give CH₃OCF (CF₃)COOMe bp 110-118°C. This was direct fluorinated according to <patcit id="pcit0023" dnum="US5488142A"><text>U.S. Patent 5,488, 142</text></patcit> and the product was methanolysed to give the same ester as in Example Reference 11. One could then convert this to the perfluorovinyl ether as described above.

Reference Example 17. Perfluoro methyl vinyl ether (not claimed)

CH₃OCF(CF₃)COOMe from Example 15 was fluorinated in an ECF cell according to <patcit id="pcit0024" dnum="US2713593A"><text>U.S. Patent 2,713,593</text></patcit> to give in 21% yield CF₃OCF(CF₃)COF. One could then convert this to the perfluorovinyl ether as described above.

Reference Example 18. Perfluoro methyl vinyl ether via 2-methoxy-2,3,3,3-tetrafluoropropionic acid anhydride (not claimed)

The adduct of HFPO and methanol from Reference Example 15 was hydrolysed to the carboxylic acid and dehydrated with P₂O₅ to give 2-methoxy-2,3,3,3-tetrafluoropropionic acid anhydride, bp 144-146° C. This was direct fluorinated according to <patcit id="pcit0025" dnum="US5488142A"><text>U.S. Patent 5,488,142</text></patcit> to give the perfluoro anhydride bp 85-88° C, methanolysis of which yielded CF₃OCF(CF₃)COOMe bp 76-78° C which was converted to CF₃-O-CF=CF₂ bp -23° C.

Reference Example 19. Perfluoro propyl vinyl ether (not claimed)

Hexafluoropropylene (36g) was added to 20.8g methyl lactate and about 0.2g KF in 50 ml DMF at 20-30°C. Distillation yielded a mixture of esters bp 64-76°C/ 55mm (7.3 kPa). This was fluorinated in an ECF cell according to <patcit id="pcit0026" dnum="US2713593A"><text>U.S. Patent 2,713,593</text></patcit> to give in about 25% yield a 2:1 mixture of C₃F₇OCF(CF₃)COF and C₃F₇OC₂ F₄COF. One could then convert these to the corresponding perfluorovinyl ethers as described above.