# US 4,374,782 A · Synthesis of trifluoroacetyl fluoride

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- Number: US 4,374,782 A
- Document ID: US4374782A
- Status: Granted
- Kind: A
- Application number: 06/275,009
- Filed: 1981-06-18
- Granted: 1983-02-22
- Earliest claimed: 1981-06-18
- Assignees: Allied Corporation
- Inventors: Louis G. Anello; Michael Van Der Puy; Martin A. Robinson; Richard E. Eibeck
- Web page: https://patentgrep.com/patent/US4374782A

## CPC

- C07C 51/58: Preparation of carboxylic acid halides
- C07C: ACYCLIC OR CARBOCYCLIC COMPOUNDS

## Abstract

A process for the preparation of trifluoroacetyl fluoride is disclosed, which comprises reacting, in the liquid phase, hexafluorothioacetone dimer in an aprotic solvent with at least a catalytic amount of an alkali metal fluoride in the presence of an oxidizing agent selected from the group consisting of Ag.sub.2 O, oxides of Pb, Sn, Ni, Co and Fe and M.sub.2 S.sub.2 O.sub.8 wherein M is an alkali metal. The preferred aprotic solvent is dimethylformamide; the preferred alkali metal fluoride is KF; and the preferred oxidizing agents are NiO, PbO.sub.2, and M.sub.2 S.sub.2 O.sub.8 wherein M is Na or K.

## Claims

### Claim 1

A process for the preparation of trifluoroacetyl fluoride, which comprises reacting, in the liquid phase under substantially dry conditions and at elevated temperatures, hexafluorothioacetone dimer in an aprotic solvent containing at least a catalytic amount of an alkali metal fluoride with an oxidizing agent selected from the group consisting of oxides of Pb, Sn, Ni, Co and Fe and M.sub.2 S.sub.2 O.sub.8 wherein M is an alkali metal.

### Claim 2 (depends on 1)

The process of claim 1 wherein the oxidizing agent is selected from the group consisting of PbO, PbO.sub.2, SnO, SnO.sub.2, FeO, Fe.sub.2 O.sub.3, NiO, CoO, Co.sub.3 O.sub.4, K.sub.2 S.sub.2 O.sub.8 and Na.sub.2 S.sub.2 O.sub.8.

### Claim 3 (depends on 2)

The process of claim 2 wherein the aprotic solvent is selected from the group consisting of acetonitrile, dimethylacetamide, dimethylformamide, dimethyl sulfoxide and N-methyl pyrrolidone.

### Claim 4 (depends on 2)

The process of claim 2 wherein the oxidizing agent is PbO.sub.2 and wherein the aprotic solvent is dimethylformamide.

### Claim 5 (depends on 2)

The process of claim 2 wherein the oxidizing agent is NiO and wherein the aprotic solvent is dimethylformamide.

### Claim 6 (depends on 2)

The process of claim 2 wherein the oxidizing agent is Na.sub.2 S.sub.2 O.sub.8 and wherein the aprotic solvent is dimethylformamide.

### Claim 7 (depends on 2)

The process of claim 2 wherein the oxidizing agent is K.sub.2 S.sub.2 O.sub.8 and wherein the aprotic solvent is dimethylformamide.

### Claim 8 (depends on 4, 5, 6, 7)

The process of claim 4 or 5 or 6 or 7 wherein the alkali metal fluoride is KF and wherein the molar ratio of hexafluorothioacetone dimer to KF is at least about 0.06:1 to about 1:1.

### Claim 9 (depends on 4, 5, 6, 7)

The process of claim 4 or 5 or 6 or 7 wherein the molar ratio of said oxides to hexafluorothioacetone dimer is about 2:1.

### Claim 10 (depends on 2)

The process of claim 2 which further comprises agitating the reaction mixture.