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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859452Generated: November 1, 2026

Triethylamine → (S)-1-(4-dimethylaminophenethyl)-3-methanesulfonyloxy-pyrrolidine

https://huagongshe.com/reaction/1859452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(S)-1-(4-dimethylaminophenethyl)-3-hydroxypyrrolidineHCID 69900648—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product(S)-1-(4-dimethylaminophenethyl)-3-methanesulfonyloxy-pyrrolidineHCID 86585524—

Reaction Steps

(S)-1-(4-dimethylaminophenethyl)-3-hydroxypyrrolidine (320 mg, 1.37 mmol) was dissolved in dichloromethane (10 ml). Triethylamine (152 mg, 1.50 mmol) and methanesulfonyl chloride (164 mg, 1.43 mmol) were added to the obtained solution under stirring under cooling on ice. They were stirred at 0° C. for 1 hour. The reaction liquid was distributed in dichloromethane and water. The organic layer was dried, and the solvent was evaporated under reduce pressure. The obtained residue was subjected to silica gel column chromatography. The product was eluted with dichloromethane and then with a solvent mixture (50:1) of dichloromethane and methanol. The appropriate fractions were combined, and the solvent was evaporated under reduced pressure to obtain (S)-1-(4-dimethylaminophenethyl)-3-methanesulfonyloxy-pyrrolidine in the form of a light yellow oil (378 mg, 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06528504B2
Source datasetuspto-grants-2003_03
ORD IDord-a6aea6b868d242b8895442c66ea8c458
Source noteuspto-grants-2003_03