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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280976Generated: October 30, 2026

3-Carbamoyl-1-(4-chlorobenzyl)pyrrolidin-2-one → 3-(Aminomethyl)-1-(4-chlorobenzyl)pyrrolidine

https://huagongshe.com/reaction/1280976

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Carbamoyl-1-(4-chlorobenzyl)pyrrolidin-2-oneHCID 18426256—
SolventTetrahydrofuranHCID 8028—
Product3-(Aminomethyl)-1-(4-chlorobenzyl)pyrrolidineHCID 1842625166.7%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of 3-carbamoyl-1-(4-chlorobenzyl)pyrrolidin-2-one (1.45 g) in THF (15 mL) was added 1.0 N BH3 in THF (25 mL). The reaction mixture was stirred at 65° C. for 15 h. After cooling to room temperature, the solvent was removed under reduced pressure. Water (30 mL) and conc. HCl (10 mL) were added and the mixture was stirred at 100° C. for 2 h and room temperature for 1 h. 2 N NaOH aqueous solution (100 mL) was added and the mixture was extracted with AcOEt (50 mL×3). The combined organic layers were dried over K2C3, filtered and concentrated. Column chromatography (SiO2, 15% CH3OH-5% Et3N in CH2Cl2) afforded 3-(aminomethyl)-1-(4-chlorobenzyl)pyrrolidine (860 mg, 19%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451842B1
Source datasetuspto-grants-2002_09
ORD IDord-124aa14bea874e86b0f8bb00566789ad
Source noteuspto-grants-2002_09