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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859446Generated: November 1, 2026

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

https://huagongshe.com/reaction/1859446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(S)-3-hydroxy-1-(4-methoxyphenethyl)pyrrolidineHCID 12148702—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product(S)-3-methanesulfonyloxy-1-(4-methoxyphenethyl)pyrrolidineHCID 12148703—

Reaction Steps

(S)-3-Hydroxy-1-(4-methoxyphenethyl)pyrrolidine (541 mg, 2.45 mmol) was dissolved in dichloromethane (15 ml). Triethylamine (272 mg, 2.69 mmol) and methanesulfonyl chloride (295 mg, 2.58 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 of dichloromethane and methanol (50:1). The appropriate fractions were combined, and the solvent was evaporated under reduced pressure to obtain (S)-3-methanesulfonyloxy-1-(4-methoxyphenethyl)pyrrolidine in the form of a white solid (734 mg, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06528504B2
Source datasetuspto-grants-2003_03
ORD IDord-54bc0494b11a41cdafa7cdddfbc33338
Source noteuspto-grants-2003_03