Organic compounds -- part of the class 532-570 series – Organic compounds – Carboxylic acids and salts thereof
Reexamination Certificate
1999-12-22
2002-11-19
Rotman, Alan L. (Department: 1625)
Organic compounds -- part of the class 532-570 series
Organic compounds
Carboxylic acids and salts thereof
C560S184000, C423S481000, C423S483000
Reexamination Certificate
active
06482979
ABSTRACT:
FIELD OF THE INVENTION
The present invention is related to perfluorinated acid fluorides, especially perfluorinated 3-alkoxy propionic acid fluorides, and a method of preparing such compounds. These compounds are valuable intermediates for e.g. vinyl ethers that can be used to prepare a variety of fluoropolymers including those having enhanced low temperature properties.
BACKGROUND OF THE INVENTION
Fluorinated vinyl ethers have found applicability in numerous fluoropolymers. For example, they may be copolymerized with tetrafluoroethylene (TFE) to produce modified polytetrafluoroethylene (mPTFE). Likewise, they may be copolymerized with a variety of other fluorinated monomers to produce fluoroplastic and/or fluoroelastomeric polymers. Some of the benefits of employing vinyl ethers in fluoropolymers are described in various review articles. See for example, Modern Fluoropolymers, John Scheirs, Wiley Series in Polymer Science, 1997. See also Emel 'yanov et al, Zh. Org. Khim (1994), 30(8), 1266-70.
There are a number of routes to prepare fluorinated vinyl ethers. Generally these routes start with perfluorinated acid fluorides. See for example Modern Fluoropolymers, J. Scheirs, Wiley Series in Polymer Science, 1997 and the literature cited therein.
Even though perfluorinated acid fluorides are commonly used in the synthesis of fluorinated vinyl ethers, there are only a few synthetic routes that are known to lead to perfluorinated 3-alkoxy propionic fluorides starting from hydrogen containing precursors.
For example, U.S. Pat. No. 2,713,593 discloses the electrochemical fluorination of a nonfluorinated carboxylic acid chloride to form perfluorinated acid fluoride.
Another synthesis route is disclosed in V. V. Berenblit et al., Zh, Prikl. Khim. (Leningrad), (1975) 48(3) 709-11. In this route a hydrocarbon ester is electrochemically fluorinated to provide the perfluorinated acid fluoride.
These synthesis routes are not entirely satisfactory because yield of acid fluoride is low, e.g., less than 15% by weight. This is in keeping with the generally low yields of ethers during electrochemical fluorination.
A third route to the synthesis of acid fluorides is disclosed in EPA 148,482 (Ohsaka et al) and EPA 290,848 (Oka et al). In this route, tetrafluorooxetane is reacted with an at least partially fluorinated acid fluoride. The resulting intermediate is fluorinated to provide a perfluorinated acid fluoride. This synthesis route has at least two disadvantages. First, the tetrafluorooxetane must be synthesized. This adds additional steps, time and cost to the synthesis of the acid fluoride. Second, the reaction of the at least partially fluorinated acid fluoride with the oxetane may result in the formation of oligomers thereby reducing the yield of the desired acid fluoride.
SUMMARY OF THE INVENTION
The present invention provides a process for the preparation of a perfluorinated acid fluoride from a partially fluorinated, hydrogen-containing starting material. The process of the present invention provides a perfluorinated acid fluoride has the formula
R
f
OCF
2
CF
2
COF (1)
wherein R
f
is a perfluorinated linear or branched monovalent aliphatic, preferably alkyl, radical that has from 1-20 (preferably from 1 to 5) carbon atoms. The method of the invention comprises the steps of
(a) providing a partially fluorinated, hydrogen-containing starting material of the formula
ROCF
2
CF
2
COZ (2).
wherein R is a monovalent, hydrogen-containing, linear or branched aliphatic (preferably alkyl) radical that may contain oxygen atoms and that contains from 1-20 (preferably from 1 to 5) carbon atoms; and Z is selected from —OH, a halogen (e.g., chlorine or fluorine) or a monovalent hydrogen-containing linear or branched alkyl or alkoxy group that contains 1-20 (preferably 1-5) carbon atoms, or an anhydride radical selected from R′COO— where R′ is selected from R or ROCF
2
CF
2
COO— where R is as defined above;
(b) fluorinating the starting material by contacting it with a fluorinating agent under conditions sufficient to replace hydrogen atoms on the starting material with fluorine; and
(c) optionally converting the product of step (b) to the perfluorinated acid fluoride.
R and Z may be partially fluorinated if desired. Additionally, R and Z may contain one or more oxygen atoms.
As it is used herein, the term perfluorinated means that all of the carbon-bonded hydrogen atoms have been replaced by fluorine.
Surprisingly, the process of the invention provides high yields (preferably 50 mole % or more) of the perfluorinated acid fluoride of the Formula (1). Prior art techniques for producing acid fluorides of formula (1) typically result in yields of the acid fluoride of substantially less than 50 mole %, typically less than 25 mole %. Additionally, the process of the invention is simple to use. It provides the desired acid fluoride in a straight forward manner.
DETAILED DESCRIPTION
The starting material for the process of the invention is the hydrogen-containing compound of the formula
ROCF
2
CF
2
COZ (2)
wherein R and Z are as described above. R and Z may be the same or different from one another. Preferably at least one of R and Z is a methyl or ethyl group. The starting materials of Formula (2) are preferably esters, anhydrides or ketones.
When the starting material for the process of the invention is an ester or an anhydride, it has the formula
ROCF
2
CF
2
COOR″ (3)
wherein R″ is a monovalent, hydrogen containing alkyl radical that contains from 1 to 20 (preferably 1 to 5) carbon atoms or
When the starting material is a ketone, it preferably has the formula
ROCF
2
CF
2
COCF
2
CF
2
OR (4)
where R is as described above.
Starting materials useful in the invention have been previously described. See, for example, U.S. Pat. No. 2,988,537 (Wiley), which disclose the reaction of tetrafluoroethylene (TFE) with a sodium alkoxylate in the presence of a dialkyl carbonate. This reaction forms a compound which may then be treated with anhydrous acid to yield a hydrogen-containing, partially fluorinated starting material of Formula (2). This reaction sequence may be graphically represented by the following:
wherein Z′ is selected from a halogen, or a monovalent hydrogen containing linear or branched alkyl group of from 1 to 20 carbon atoms, and R is as defined above.
See also U.S. Pat. No. 5,235,094 (Darst et al) which discloses another route to the synthesis of a partially fluorinated ester of Formula (3).
The partially fluorinated esters of Formula (3) can be transformed to corresponding anhydrides using procedures well-known to those skilled in the art.
The partially fluorinated starting material is fluorinated by contacting it with fluorine to form an intermediate in which all of the hydrogen atoms present on the starting material are replaced with fluorine. This is done under conditions that are appropriate to replace the hydrogen on the starting material, but not so aggressive that backbone of the starting material is disturbed.
Fluorination of the starting material can be accomplished by a number of techniques. Examples of useful fluorination techniques include electrochemical fluorination (ECF) and direct fluorination (DF).
Electrochemical fluorination is a well known technique that is disclosed in a number of publications including U.S. Pat. No. 2,713,593 and WO 98/50603. It is a process that employs hydrogen fluoride. Electrochemical fluorination of the starting material results directly in the desired perfluorinated acid fluoride of Formula (1). As a result, there is no need to convert the product of this step any further. Surprisingly, the use of the partially fluorinated precursor of Formula (2) as the starting material results in unexpectedly high yields of the acid fluoride.
Direct fluorination is another well known technique. This technique is disclosed in a host of articles and patents. See for example, U.S. Pat. No. 5,488,142 (Fall et al); U.S. Pat. No. 4,523,039 (Lagow et al); Kirk Othmer Encyclopedia
Gross Christopher L.
Hintzer Klaus
Moore George G. I.
Qiu Zai-Ming
Schulz Jay F.
Dyneon LLC
Lilly James V.
Reyes Hector M
Rotman Alan L.
Szymanski Brian E.
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