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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1983732Generated: November 1, 2026

4-Chloro-2-nitrobenzaldehyde → HCID 66758130, compound

https://huagongshe.com/reaction/1983732

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-2-nitrobenzaldehydeHCID 79674—
Reactant1-Boc-3-aminopyrrolidineHCID 2756370—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductHCID 66758130HCID 66758130—

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-2-nitro-benzaldehyde (1.98 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=1.28, ES+; 356)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07541365B2
Source datasetuspto-grants-2009_06
ORD IDord-0e8e480bc0554d5ba9f4ae5a6e6409b9
Source noteuspto-grants-2009_06