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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492277Generated: October 25, 2026

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

https://huagongshe.com/reaction/492277

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 numberUS07531689B2
Source datasetuspto-grants-2009_05
ORD IDord-daa31aa198fd43f28910e7fc0418ebc5
Source noteuspto-grants-2009_05