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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133570Generated: October 30, 2026

Acetonitrile → 2-Carbamoyl-1-(4-chlorobenzyl)pyrrolidine

https://huagongshe.com/reaction/133570

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
Reactant1-Chloro-4-(chloromethyl)benzeneHCID 7723—
ReactantTriethylamineHCID 8471—
ReactantPyrrolidine-2-carboxamide hydrochlorideHCID 3016353—
SolventDichloromethaneHCID 6344—
Product2-Carbamoyl-1-(4-chlorobenzyl)pyrrolidineHCID 18426272—

Reaction Conditions

Temperature70 °C

Reaction Steps

Triethylamine (7.45 mL) and 4-chlorobenzyl chloride (3.88 g, 24.1 mmol) were added to an acetonitrile (35 mL) solution of dl-prolinamide hydrochloride (2.5 g, 21.8 mmol). The resulting reaction mixture was stirred at 70° C. for 4 hours and subsequently stirred at 25° C. for 16 hours. The resulting mixture was diluted with dichloromethane (20 mL) and washed with water (30 mL×3). The organic layer was dried (over MgSO4) and concentrated. The obtained crude product was purified by chromatography (SiO2, methanol-dichloromethane) to thereby provide 2-carbamoyl-1-(4-chlorobenzyl)pyrrolidine (5.21 g, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07390830B1
Source datasetuspto-grants-2008_06
ORD IDord-27212f5383af45468743ef003e9abb01
Source noteuspto-grants-2008_06