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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1475620Generated: October 30, 2026

tert-Butyl 1-[3-(benzylamino)benzyl]cyclopropanecarboxylate → tert-Butyl 1-(3-aminobenzyl)cyclopropanecarboxylate

https://huagongshe.com/reaction/1475620

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 1-[3-(benzylamino)benzyl]cyclopropanecarboxylateHCID 58136299—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 1-(3-aminobenzyl)cyclopropanecarboxylateHCID 58136514—

Reaction Steps

6.98 g (22.43 mmol) of tert-butyl 1-[3-(benzylamino)benzyl]cyclopropanecarboxylate were dissolved in 50 ml of ethanol and 50 ml THF, and 0.48 g (0.45 mmol) of palladium (10% on carbon) were added. At RT, the mixture was stirred under a hydrogen atmosphere at atmospheric pressure for 2 h. The reaction mixture was then filtered off with suction through kieselguhr, the residue was washed with THF and the filtrate was concentrated. The crude product was purified by chromatography on silica gel (mobile phase cyclohexane/ethyl acetate 10:1). This gave 3.66 g (65.9% of theory) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018258B2
Source datasetuspto-grants-2015_04
ORD IDord-556e49ec71f245868de43ad3a11ed1ff
Source noteuspto-grants-2015_04