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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703Generated: October 25, 2026

Carbon Dioxide → 2,2,2-Trifluoroethyl trifluoromethanesulfonate

https://huagongshe.com/reaction/1703

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
Reactant2,2,2-TrifluoroethanolHCID 6409—
ReactantTriethylamineHCID 8471—
ReactantTrifluoromethanesulfonyl chlorideHCID 79000—
SolventDiethyl EtherHCID 3283—
SolventIsopropanolHCID 3776—
SolventDichloromethaneHCID 6344—
Product2,2,2-Trifluoroethyl trifluoromethanesulfonateHCID 80366—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of trifluoromethanesulfonyl chloride (800 uL, 7.5 mmole) in CH2Cl2 (6 mL) was cooled under argon to -60° C. (IPA:dry ice bath). 2,2,2-Trifluoroethanol was added (456 uL, 6 mmol) and triethylamine (1.04 uL, 7.5 mmol) was added dropwise. The reaction was stirred for 1.5 hours then warmed to 0° C. for 1 hour. Anhydrous ether (20 mL) was added and the mixture was stirred at 0° C. for 30 minutes. The solids were filtered off and the solvent was removed under reduced pressure with the flask maintained at 0° C. This afforded the 2,2,2-trifluoroethyltriflate as a yellow oil which was used immediately.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05726172
Source datasetuspto-grants-1998_03
ORD IDord-c1eb50330c204669ac80b93517bb8dec
Source noteuspto-grants-1998_03