GB858671A - Fluorocarbon acid and derivatives - Google Patents
Fluorocarbon acid and derivativesInfo
- Publication number
- GB858671A GB858671A GB12753/57A GB1275357A GB858671A GB 858671 A GB858671 A GB 858671A GB 12753/57 A GB12753/57 A GB 12753/57A GB 1275357 A GB1275357 A GB 1275357A GB 858671 A GB858671 A GB 858671A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- prepared
- oxydipropionyl
- fluoride
- salt
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/235—Saturated compounds containing more than one carboxyl group
- C07C59/305—Saturated compounds containing more than one carboxyl group containing ether groups, groups, groups, or groups
- C07C59/315—Saturated compounds containing more than one carboxyl group containing ether groups, groups, groups, or groups containing halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/125—Saturated compounds having only one carboxyl group and containing ether groups, groups, groups, or groups
- C07C59/135—Saturated compounds having only one carboxyl group and containing ether groups, groups, groups, or groups containing halogen
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
Abstract
The invention comprises perfluoro-oxydipropionic acid O(CF2CF2COOH)2 and its acid halides, metal and ammonium salts and alkyl esters. The acid may be prepared by electrolytically fluorinating an oxydipropionyl halide with liquid hydrogen fluoride in a nickel anode cell to give perfluoro-oxydipropionyl fluoride and hydrolysing this to the acid. In an example perfluoro-oxydipropionyl fluoride is obtained electrolytically from oxydipropionyl fluoride, the acid is obtained by adding a slurry of calcium oxide and acidifying the resulting calcium salt with sulphuric acid. An alternative work-up involves the isolation of a sodium salt which is acidified as before. The silver salt is prepared using silver oxide and the carboxylate groups are then replaced by iodine to give a compound O(CF2CF2I)2. The mercury salt is prepared using mercuric oxide, the ethyl ester is prepared using ethanol and the methyl ester is prepared from the sodium salt using methyl-p-toluene sulphonate. Mono decarboxylation to give omega-hydroperfluoro-ethoxypropionic acid by heating the acid with piperidine is also described. A method for the preparation of the acid chloride, bromide and iodide is also mentioned. Specifications 686,678 and 735,730 are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US858671XA | 1956-04-23 | 1956-04-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB858671A true GB858671A (en) | 1961-01-11 |
Family
ID=22194488
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB12753/57A Expired GB858671A (en) | 1956-04-23 | 1957-04-18 | Fluorocarbon acid and derivatives |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB858671A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6753380B2 (en) | 2001-03-09 | 2004-06-22 | 3M Innovative Properties Company | Water-and oil-repellency imparting ester oligomers comprising perfluoroalkyl moieties |
US6803109B2 (en) | 2001-03-09 | 2004-10-12 | 3M Innovative Properties Company | Water-and oil-repellency imparting urethane oligomers comprising perfluoroalkyl moieties |
US7301052B2 (en) | 2003-02-21 | 2007-11-27 | Asahi Glass Company, Linited | Process for producing perfluorodiacyl fluorinated compounds |
-
1957
- 1957-04-18 GB GB12753/57A patent/GB858671A/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6753380B2 (en) | 2001-03-09 | 2004-06-22 | 3M Innovative Properties Company | Water-and oil-repellency imparting ester oligomers comprising perfluoroalkyl moieties |
US6803109B2 (en) | 2001-03-09 | 2004-10-12 | 3M Innovative Properties Company | Water-and oil-repellency imparting urethane oligomers comprising perfluoroalkyl moieties |
US7301052B2 (en) | 2003-02-21 | 2007-11-27 | Asahi Glass Company, Linited | Process for producing perfluorodiacyl fluorinated compounds |
US7501540B2 (en) | 2003-02-21 | 2009-03-10 | Asahi Glass Company, Limited | Process for producing perfluorodiacyl fluorinated compounds |
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