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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1983738Generated: November 2, 2026

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

https://huagongshe.com/reaction/1983738

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 numberUS07541365B2
Source datasetuspto-grants-2009_06
ORD IDord-de751553fe354aa28a27724bf13ab582
Source noteuspto-grants-2009_06