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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713858Generated: November 1, 2026

Ethyl 3-(4-nitrobenzyl)cyclobutanecarboxylate → Ethyl 3-(4-aminobenzyl)cyclobutanecarboxylate

https://huagongshe.com/reaction/1713858

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-(4-nitrobenzyl)cyclobutanecarboxylateHCID 59464076—
SolventEthyl AcetateHCID 8857—
ProductEthyl 3-(4-aminobenzyl)cyclobutanecarboxylateHCID 5946416850%

Reaction Steps

Ethyl 3-(4-nitrobenzyl)cyclobutanecarboxylate (4.02 mmol) was stirred in EtOAc (20 mL) at room temperature and nitrogen was bubbled through. 10% Palladium on carbon (160 mg) was added and the reaction vessel was put under an atmosphere of hydrogen. The mixture was stirred overnight then filtered through diatomaceous earth and concentrated by evaporation under reduced pressure. The residue was purified by chromatography eluting with 0-55% EtOAc/isohexane to give the title compound (466 mg, 50%) as an oil; 1H NMR δ 1.15-1.20 (3H, m), 1.77-1.94 (2H, m), 2.13-2.20 (2H, m), 2.33-2.37 (2H, m), 2.43-2.46 (1H, m), 2.53-2.56 (1H, m), 2.92-3.07 (1H, m), 4.01-4.08 (2H, m), 4.77 (2H, d), 6.46-6.49 (2H, m), 6.78-6.82 (2H, m); MS m/e M+MeCN 275.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795283B2
Source datasetuspto-grants-2010_09
ORD IDord-b4d0eb53e10742b894d5f1644f5efc1b
Source noteuspto-grants-2010_09