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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2194559Generated: November 1, 2026

4-Toluenesulfonyl chloride → Tetrahydrofuran-3-YL 4-methylbenzenesulfonate, (3R)-

https://huagongshe.com/reaction/2194559

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant(-)-3-HydroxytetrahydrofuranHCID 641512—
SolventDichloromethaneHCID 6344—
ProductTetrahydrofuran-3-YL 4-methylbenzenesulfonate, (3R)-HCID 1114919783.3%

Reaction Steps

To a mixture of (R)-tetrahydrofuran-3-ol (1 g, 11.4 mmole) and TEA (2.3 g, 22.8 mmole) in DCM (20 mL) at 0° C. was added dropwise 4-methylbenzene-1-sulfonyl chloride (2.2 g, 11.4 mmole). The resulting mixture was stirred at room temperature for 8 h. The mixture was washed with water, dried over MgSO4, filtered, and concentrated. The crude product was purified by ISCO (silica gel, eluting with 15% ethyl acetate in hexane) to give the title compound (2.3 g). MS (ESI) m/z: Found: 243.3 (M++1). Calc. 242.3 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08334292B1
Source datasetuspto-grants-2012_12
ORD IDord-b5b571d0b54e4110949d6027a41e8b51
Source noteuspto-grants-2012_12