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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2280629Generated: November 1, 2026

Triethylamine → (S)-tetrahydrofuran-3-yl methanesulfonate

https://huagongshe.com/reaction/2280629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(S)-(+)-3-HydroxytetrahydrofuranHCID 2733227—
SolventDichloromethaneHCID 6344—
Product(S)-tetrahydrofuran-3-yl methanesulfonateHCID 5756158892.5%

Reaction Steps

(S)-Tetrahydrofuran-3-ol 2a (300 mg, 3.40 mmol) and triethylamine (687 mg, 6.80 mmol) were dissolved in 20 mL of dichloromethane in an ice bath, followed by addition of methanesulfonyl chloride (908 mg, 7.93 mmol). The reaction solution was warmed up to room temperature and stirred for 2 hours. The resulting solution was mixed with 10 mL of dichloromethane, washed with water (30 mL×2), dried with anhydrous magnesium sulphate, and filtered. The filtrate was concentrated under reduced pressure to obtain the crude title compound (S)-tetrahydrofuran-3-yl methanesulfonate 2b as a yellow oil (522 mg, yield 92.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139548B2
Source datasetuspto-grants-2015_09
ORD IDord-e1fb6075bf03430ca64d3ab781cae1be
Source noteuspto-grants-2015_09