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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010990Generated: November 1, 2026

Triethylamine → 2-(Tetrahydro-3-furanyl)ethyl methanesulfonate

https://huagongshe.com/reaction/1010990

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium BicarbonateHCID 516892—
Reactant2-(Oxolan-3-yl)ethan-1-olHCID 11126225—
SolventDichloromethaneHCID 6344—
Product2-(Tetrahydro-3-furanyl)ethyl methanesulfonateHCID 57699822—

Reaction Steps

2-(Tetrahydro-3-furanyl)ethanol (230 mg) was dissolved in dry DCM (5 mL) and triethylamine (0.552 mL) was added. The stirred solution was cooled (ice bath) under nitrogen and methanesulphonyl chloride (0.199 mL) was added dropwise over 5 mins. The mixture was allowed to warm slowly to room temperature as the ice bath melted and was left for 16 h. The mixture was shaken with saturated sodium bicarbonate solution and the aqueous layer was extracted with DCM (×2). The combined organics were washed with brine, dried using a hydrophobic frit and evaporated to give the title compound (364 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977344B2
Source datasetuspto-grants-2011_07
ORD IDord-6d6052d02976479ead74394d279bfd66
Source noteuspto-grants-2011_07