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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178841Generated: October 25, 2026

Difluoro(fluorosulphonyl)acetyl fluoride → CH2=C(CF2Ocf2CF2SO2F)2

https://huagongshe.com/reaction/1178841

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDifluoro(fluorosulphonyl)acetyl fluorideHCID 69614—
ReactantPotassium FluorideHCID 522689—
ReactantCH2=C(CF2Oso2F)2HCID 10471472—
ReactantHCID 178527443HCID 178527443—
SolventWaterHCID 962—
SolventDiglymeHCID 8150—
ProductCH2=C(CF3)CF2Oso2FHCID 87741755—
ProductCH2=C(CF2Ocf2CF2SO2F)2HCID 13172662558%

Reaction Conditions

Temperature20 °C

Reaction Steps

CH2═C(CF2OSO2F)2 is added gradually to FSO2CF2CF2OK, which is prepared from freshly dried KF (3.9 g, 0.067 mole) and FSO2CF2COF (12 g, 0.067 mole) in dry diglyme (30 ml). The resulting mixture is stirred 3 hours at 20° C. The reaction mixture is poured into water. The organic layer is washed with aqueous sodium bicarbonate, then water, and then dried over MgSO4. Distillation gives CH2═C(CF3)CF2OSO2F (0.5 g) and CH2═C(CF2OCF2CF2SO2F)2 (9 g, 58% yield, b.pt. 95–96° C. at 15 mm Hg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07276624B2
Source datasetuspto-grants-2007_10
ORD IDord-2a360d231027458abc5d04db8e2f8c79
Source noteuspto-grants-2007_10