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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917169Generated: November 1, 2026

4-Chlorobenzaldehyde → 3-(4-Chloro-benzylamino)-pyrrolidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/917169

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorobenzaldehydeHCID 7726—
Reactant1-Boc-3-aminopyrrolidineHCID 2756370—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product3-(4-Chloro-benzylamino)-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 66757670—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3-Amino-pyrrolidine-1-carboxylic acid tert-butyl ester (2 g, 10.7 mmol) in methanol (20 mL) was added 4-Chloro-benzaldehyde (1.5 g, 10.7 mmol). The resultant solution was heated at 60° C. overnight. The reaction mixture was cooled to 0° C. and to it was added NaBH4 (629 mg, 10 mmol). After 1 h, the reaction solution was quenched with saturated NaHCO3 solution and extracted with ethyl acetate. The organic extract was dried over MgSO4, filtered and concentrated to provide the crude product as an oil. The crude product was used in the subsequent reaction without further purification. LCMS (retention time=1.27, ES+311).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07271176B2
Source datasetuspto-grants-2007_09
ORD IDord-ce1efdee027744cd9b1057e509e80b42
Source noteuspto-grants-2007_09