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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19322Generated: October 26, 2026

Triethylamine → 2,2-Difluoroethyl trifluoromethanesulfonate

https://huagongshe.com/reaction/19322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
Reactant2,2-Difluoroethan-1-olHCID 136187—
SolventDichloromethaneHCID 6344—
Product2,2-Difluoroethyl trifluoromethanesulfonateHCID 277408975%

Reaction Conditions

Temperature25 °C

Reaction Steps

In a flask under argon was placed triflic anhydride (10.22 mL, 61 mmol) and dichloromethane (10 mL) and it was cooled to −70° C. To this cooled mixture was added slowly a solution of 2,2-difluoroethanol (5.00 g, 61 mmol) and triethylamine (8.5 mL, 61 mmol) in dichloromethane (10 mL). After the addition was complete, the mixture was warmed to 25° C. and then concentrated in vacuo. This material was distilled at 60° C. and 50 mm Hg which afforded trifluoro-methanesulfonic acid 2,2-difluoro-ethyl ester (9.74 g, 75%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741327B2
Source datasetuspto-grants-2010_06
ORD IDord-7ce4d0728fee45208e0af46ba190a52b
Source noteuspto-grants-2010_06