Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648955Generated: October 25, 2026

Tetrafluoroethylene → FSO2CF2CF2OCF2CF2Br

https://huagongshe.com/reaction/1648955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrafluoroethyleneHCID 8301—
ReactantBromineHCID 24408—
ReactantDifluoro(fluorosulphonyl)acetyl fluorideHCID 69614—
ReactantPotassium FluorideHCID 522689—
ReactantSodium BisulfiteHCID 23665763—
SolventAcetonitrileHCID 6342—
SolventCfc 113HCID 6428—
ProductFSO2CF2CF2OCF2CF2BrHCID 13311567—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 5.8 g potassium fluoride, 60 ml acetonitrile and 12 ml fluorosulfonyl difluoroacetyl fluoride was heated at 80° C. for one hour. The resulting mixture was placed in a stainless steel autoclave and heated at 50° C. for one hour and 80° C. for one hour with 16 g of bromine and 30 g of tetrafluoroethylene. The reaction mixture was poured into a solution of sodium bisulfite, 50 ml 1,1,2-trichloro-1,2,2-trifluoroethane was added and the mixture was distilled to give a distillate boiling up to 100° C. which contained two layers. The organic layer was separated and distilled to give FSO2CF2CF2OCF2CF2Br, b.p. 106°, confirmed by infrared, nuclear magnetic resonance and mass spectroscopy.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04414280
Source datasetuspto-grants-1983_11
ORD IDord-4ff494e2acf84bd7b010e48613ebf165
Source noteuspto-grants-1983_11