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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273852Generated: October 31, 2026

Triethylamine → 2-[2-(2,2,2-Trifluoroethoxy)phenoxy]ethyl Methanesulfonate

https://huagongshe.com/reaction/273852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2-[2-(2,2,2-Trifluoroethoxy)phenoxy]ethanolHCID 10776163—
SolventDichloromethaneHCID 6344—
Product2-[2-(2,2,2-Trifluoroethoxy)phenoxy]ethyl MethanesulfonateHCID 10519307—

Reaction Steps

To a solution of 2-[2-(2,2,2-trifluoroethoxy)phenoxy]ethanol (210 mg) in methylene chloride (1 ml) were added triethylamine (186 μl) and methanesulfonyl chloride (83 μl) with stirring under ice cooling, and the mixture was reacted at room temperature for 30 minutes. The reaction mixture was concentrated under reduced pressure. To the concentrate was added water, and the mixture was extracted with diethyl ether. The extract was washed with water, dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by medium pressure liquid column chromatography on silica gel using a mixture of hexane and ethyl acetate (2/1) as eluent to give 273 mg of 2-[2-(2,2,2-trifluoroethoxy)phenoxy]ethyl methansulfonate melting at 40.5°-42.0° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05387603
Source datasetuspto-grants-1995_02
ORD IDord-68eaa92338f647288ba099d25bf70c98
Source noteuspto-grants-1995_02