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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373651Generated: November 1, 2026

Triethylamine → 2-[3-(2-Oxo-1-pyrrolidinyl)phenyl]ethyl methanesulfonate

https://huagongshe.com/reaction/2373651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1-[3-(2-Hydroxyethyl)phenyl]-2-pyrrolidinoneHCID 57444361—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product2-[3-(2-Oxo-1-pyrrolidinyl)phenyl]ethyl methanesulfonateHCID 5744436293%

Reaction Steps

Methanesulfonyl chloride (0.124 mL) was added dropwise to a stirred solution of 1-[3-(2-hydroxyethyl)phenyl]-2-pyrrolidinone (0.30 g) and triethylamine (0.42 mL) in dichloromethane (10 mL) at room temperature under an inert atmosphere. The solution was stirred for 2 hours. The reaction mixture was diluted with ethyl acetate (50 mL) and washed with water (50 mL), aqueous hydrochloric acid (1N, 2×50 mL), a saturated aqueous solution of sodium hydrogencarbonate (50 mL) and brine (50 mL). The organic layer was dried over sodium sulfate and concentrated under reduced pressure. The crude was purified by flash chromatography on silica gel, eluting with ethyl acetate-cyclohexane (50:50) to afford the title compound in 93% yield (0.384 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07459456B2
Source datasetuspto-grants-2008_12
ORD IDord-cff7f06c7af04405b7942b9b1928244e
Source noteuspto-grants-2008_12