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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52184Generated: October 26, 2026

Water → 2-Thienylmethyl methanesulfonate

https://huagongshe.com/reaction/52184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2-ThiophenemethanolHCID 69467—
SolventDichloromethaneHCID 6344—
Product2-Thienylmethyl methanesulfonateHCID 1897343038%

Reaction Steps

To a 0° C. mixture of 2-thiophenemethanol (2.80 g, 24.5 mmol) and triethylamine (5.10 mL, 36.8 mmol) in CH2Cl2 (25 mL) was added methanesulfonyl chloride (2.09 mL, 27.0 mmol) and the reaction mixture was stirred for 2 hours. The reaction mixture was poured into H2O and the layers were separated. The organic phase was washed with cold 1N HCl (3×), saturated aqueous NaHCO3, and brine, dried over MgSO4, filtered. and concentrated in vacuo. 2-thienylmethyl methanesulfonate (1.78 g, 38%) was obtained by chromatography on silica gel (20% ethyl acetate/hexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616596
Source datasetuspto-grants-1997_04
ORD IDord-7a6e7ff6416e4d33a0570bba9e53735b
Source noteuspto-grants-1997_04