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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822803Generated: November 1, 2026

Tetrahydrofurfuryl alcohol → (Tetrahydrofuran-2-yl)methyl methanesulfonate

https://huagongshe.com/reaction/1822803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofurfuryl alcoholHCID 7360—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
SolventDichloromethaneHCID 6344—
Product(Tetrahydrofuran-2-yl)methyl methanesulfonateHCID 26611992%

Reaction Conditions

Temperature0 °C

Reaction Steps

Tetrahydrofurfuryl alcohol (2.01 g, 19.7 mmol, 1.0 eq.) was dissolved in dichloromethane (100 mL) under an argon atmosphere, cooled to 0° C. and treated sequentially with triethylamine (3.02 mL, 21.7 mmol, 1.1 eq) and methanesulfonyl chloride (1.60 mL, 20.7 mmol, 1.05 eq.). The ice bath was removed and stirring continued for 14 h before the mixture was poured into a separatory funnel containing water. The phases were separated and the organic layer was washed with water (4×), dried on MgSO4, filtered and concentrated in vacuo to yield 3.26 g [92%] of tetrahydrofurfuryl methanesulfonate as a crude pale yellow oil, used in the subsequent displacement step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07037916B2
Source datasetuspto-grants-2006_05
ORD IDord-72aac5e214b64d28bf5983b6320d93b9
Source noteuspto-grants-2006_05