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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2076411Generated: November 1, 2026

Triethylamine → (Tetrahydrofuran-3-yl)methyl methanesulfonate

https://huagongshe.com/reaction/2076411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantTetrahydro-3-furanmethanolHCID 139980—
ReactantSodium BicarbonateHCID 516892—
SolventDichloromethaneHCID 6344—
Product(Tetrahydrofuran-3-yl)methyl methanesulfonateHCID 2227301099%

Reaction Steps

To a stirring solution of (3-oxolanyl)methan-1-ol (25 g, 245 mmol) and triethylamine (34.37 mL, 245 mmol) in dry dichloromethane (250 mL) at 0° C. under N2 atmosphere was added dropwise methanesulfonyl chloride (18.94 mL, 245 mmol). The reaction mixture was stirred overnight after warming to room temperature, then a saturated solution of NaHCO3 (100 mL) was added and the mixture stirred for another 30 min. The biphasic mixture was separated and the organic layer was discarded. The aqueous layer was extracted with dichloromethane (3×25 mL) and the combined dichloromethane extracts were dried (Na2SO4), filtered and concentrated by rotary evaporation to give 42.16 g of (3-oxolanyl)methyl methanesulfonate (99%) as a light brown liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07923559B2
Source datasetuspto-grants-2011_04
ORD IDord-e3e51fd249074cd196946eaa786bfca0
Source noteuspto-grants-2011_04