Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1475670Generated: October 30, 2026

(+/-)-tert-Butyl 1-{[3-(benzylamino)-4-chlorophenyl](methoxy)methyl}cyclopropanecarboxylate → (+/-)-tert-Butyl 1-[(3-amino-4-chlorophenyl)(methoxy)methyl]cyclopropanecarboxylate

https://huagongshe.com/reaction/1475670

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(+/-)-tert-Butyl 1-{[3-(benzylamino)-4-chlorophenyl](methoxy)methyl}cyclopropanecarboxylateHCID 68170328—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product(+/-)-tert-Butyl 1-[(3-amino-4-chlorophenyl)(methoxy)methyl]cyclopropanecarboxylateHCID 68170329—

Reaction Steps

6.20 g (15.4 mmol) of (+/−)-tert-butyl 1-{[3-(benzylamino)-4-chlorophenyl](methoxy)methyl}-cyclopropanecarboxylate were dissolved in 300 ml of ethyl acetate and inertized with argon, and 350 mg of palladium (10% on carbon) were added. At RT, the reaction mixture was stirred for a total of 24 h under an atmosphere of hydrogen at atmospheric pressure. The reaction mixture was then filtered through Celite, the residue was washed thoroughly with ethyl acetate and the combined filtrate was concentrated under reduced pressure. The crude product was purified by chromatography on silica gel (mobile phase cyclohexane/ethyl acetate 30:1→10:1). This gave 3.36 g of the target compound (69.9% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018258B2
Source datasetuspto-grants-2015_04
ORD IDord-0446f913827744b7a20fd5d7a9bd60d9
Source noteuspto-grants-2015_04