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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2251906Generated: November 1, 2026

Triethylamine → (S)-3-methanesulfonyloxy-1-(3-pyrrolidinophenethyl)pyrrolidine

https://huagongshe.com/reaction/2251906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium BicarbonateHCID 516892—
Reactant(S)-3-hydroxy-1-(3-pyrrolidinophenethyl)pyrrolidineHCID 69199429—
SolventDichloromethaneHCID 6344—
Product(S)-3-methanesulfonyloxy-1-(3-pyrrolidinophenethyl)pyrrolidineHCID 86592731—

Reaction Steps

(S)-3-Hydroxy-1-(3-pyrrolidinophenethyl)pyrrolidine (1.04 g, 4.00 mmol) was dissolved in dichloromethane (10 ml). Triethylamine (0.76 ml, 5.49 mmol) and methanesulfonyl chloride (0.39 ml, 5.03 mmol) were added to the obtained solution at 0° C. and they were stirred overnight. The reaction mixture was distributed into 5% aqueous sodium hydrogencarbonate solution and dichloromethane. The organic layer was dried and the solvent was evaporated under reduced pressure. The residue was subjected to the silica gel column chromatography. After the elution with chloroform and methanol (95:5), suitable fractions were collected and the solvent was evaporated under reduced pressure to obtain (S)-3-methanesulfonyloxy-1-(3-pyrrolidinophenethyl)pyrrolidine in the form of a light yellow oily substance (1.30 g, 96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07320973B2
Source datasetuspto-grants-2008_01
ORD IDord-c4f2ec73e38447bb8eff78300736474a
Source noteuspto-grants-2008_01