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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844308Generated: October 31, 2026

Trifluoromethanesulfonic anhydride → 2,2-Difluoroethyl trifluoromethanesulfonate

https://huagongshe.com/reaction/1844308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
Reactant2,2-Difluoroethan-1-olHCID 136187—
ReactantSodium BicarbonateHCID 516892—
SolventDiethyl EtherHCID 3283—
Product2,2-Difluoroethyl trifluoromethanesulfonateHCID 277408964.1%

Reaction Conditions

Temperature84 °C

Reaction Steps

Triflic anhydride (27.9 g, 99.1 mmol) was placed in a flask and cooled with an ice bath. 2,2-Difluoroethanol (8.1 g, 99.1 mmol) was added and the reaction was heated to 84° C. for 1 hour. The reaction, was cooled in an ice bath and poured into 100 ml cold 5% NaHCO3 solution. The mixture was attracted with diethyl ether, dried over MgSO4, and concentrated under reduced pressure to remove the ether. The residue was vacuum distilled to give 2,2-difluoroethyl trifluoromethanesulfonate as a clear liquid (13.6 g, 64%, bp −55° C.). 1H NMR (400 MHz, CDCl3) δ ppm 6.17-5.88 (1H), 4.61-4.13 (2H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946413B2
Source datasetuspto-grants-2015_02
ORD IDord-1b106d1b53ef4ab082cb38b7c0cce862
Source noteuspto-grants-2015_02