Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1475626Generated: October 30, 2026

tert-Butyl 1-[3-(benzylamino)-4-chlorobenzyl]cyclopropanecarboxylate → tert-Butyl 1-(3-amino-4-chlorobenzyl)cyclopropanecarboxylate

https://huagongshe.com/reaction/1475626

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 1-[3-(benzylamino)-4-chlorobenzyl]cyclopropanecarboxylateHCID 68006927—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl 1-(3-amino-4-chlorobenzyl)cyclopropanecarboxylateHCID 67957815—

Reaction Steps

50.0 g (134.4 mmol) of tert-butyl 1-[3-(benzylamino)-4-chlorobenzyl]cyclopropanecarboxylate were dissolved in 1.5 liters of ethyl acetate, and 1.43 g (1.34 mmol) of palladium (10% on carbon) were added. The reaction mixture was stirred at RT overnight under a hydrogen atmosphere at atmospheric pressure. The reaction mixture was then filtered off with suction through kieselguhr and the filtrate was concentrated. The crude product was purified by chromatography on silica gel (mobile phase petroleum ether/ethyl acetate 10:1). The product obtained was triturated using a methanol/water mixture (70:30) and the solid was isolated. This gave 24.3 g (64.1% of theory) of the target compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018258B2
Source datasetuspto-grants-2015_04
ORD IDord-24c1b06f30f64039b0cd660d4c0fb54b
Source noteuspto-grants-2015_04