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US4287124A Expired / Lapsed US ⏱️ 0.0 years remaining

Process for the preparation of 4,5-perfluoro-1,3-dioxalanes

Assignee: Hoechst AG
•
Filing: 1980-02-19
•
Granted: 1981-09-01
•
Expires: 2000-02-19
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Abstract

Abstract 4,5-Perfluoro-1,3-dioxolanes prepared by the described process have an anesthetic effect.

Inventors

  • 👤 Gunter Siegemund
  • 👤 Herbert Muffler

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-29 13:32
CPC Classifications
C; C07; C07D; C07D317/00; C07D317/08; C07D317/10; C07D317/32; C07D317/42

Claims Analysis

Total Claims: 6
Claim 1
Independent Claim 103 words
A process for the manufacture of 4,5-perfluoro-1,3-dioxolanes of the formula ##STR12## in which X and Y, independent of one another, are fluorine or trifluoromethyl and R 1 and R 2 are hydrogen or methyl, which comprises reacting a 2-(α-chloroalkoxy)-perfluorocarboxylic acid halide of the formula R.sup.1 R.sup.2 CCl--O--CXY--COZ in which X, Y, R 1 and R 2 are as defined above and Z is chlorine or fluorine, with a fluoride selected from the group consisting of potassium fluoride, cesium fluoride, ammonium fluoride and alkylammonium fluoride, under anhydrous conditions, the reaction being conducted at a temperature in the range of from 0° to 120° C.
Claim 2
Dependent Claim 103 words
A process for the manufacture of 4,5-perfluoro-1,3-dioxolanes of the formula ##STR12## in which X and Y, independent of one another, are fluorine or trifluoromethyl and R 1 and R 2 are hydrogen or methyl, which comprises reacting a 2-(α-chloroalkoxy)-perfluorocarboxylic acid halide of the formula R.sup.1 R.sup.2 CCl--O--CXY--COZ in which X, Y, R 1 and R 2 are as defined above and Z is chlorine or fluorine, with a fluoride selected from the group consisting of potassium fluoride, cesium fluoride, ammonium fluoride and alkylammonium fluoride, under anhydrous conditions, the reaction being conducted at a temperature in the range of from 0° to 120° C.
Claim 3
Dependent Claim 33 words
The process of claim 1, wherein the fluoride reacted is present in an excess of 10 to 50 mol %, calculated on the gram-atoms of chlorine present per mol of 2-(α-chloroalkoxy)-perfluorocarboxylic acid halide.
Claim 4
Dependent Claim 19 words
The process of claim 1, wherein said reaction is carried out in the presence of an aprotic polar solvent.
Claim 5
Dependent Claim 25 words
The process of claim 3, wherein said aprotic polar solvent is selected from the group consisting of nitrile, acid amide, polyether, dimethyl sulfoxide and sulfolane.
Claim 6
Dependent Claim 26 words
The process of claim 3, wherein said aprotic polar solvent is selected from the group consisting of nitrile, dimethyl formamide, dioxane and diethylene glycol dimethyl ether.

References Cited (Backward Citations)

US2260261A Cited
US3629323A Cited
US3475457A Cited
US3475456A Cited
US3758510A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1984-08-31 1985-03-02 1985-09-01 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1988-08-31 1989-03-02 1989-09-01 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1992-08-31 1993-03-02 1993-09-01 $7700.00 Window Closed / Lapsed

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