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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1779087Generated: November 2, 2026

Methyl 1-(4-nitrophenyl)cyclobutylcarbamate → Methyl 1-(4-aminophenyl)cyclobutylcarbamate

https://huagongshe.com/reaction/1779087

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 1-(4-nitrophenyl)cyclobutylcarbamateHCID 86712723—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductMethyl 1-(4-aminophenyl)cyclobutylcarbamateHCID 86712724—

Reaction Steps

A suspension of Pd/C (10%) (120 mg) and methyl 1-(4-nitrophenyl)cyclobutylcarbamate (A118) (404 mg, 1.61 mmol) in MeOH (17.0 mL) was vigorously stirred overnight under a hydrogen atmosphere. The resulting mixture was filtered through Celite then the filtrate concentrated in vacuo. The residue was purified using silica gel column chromatography (CombiFlash Rf, SiO2 cartridge, 0-75% EtOAc in cyclohexane) to give the title compound A119 (237 mg, 67%); 1H NMR (300 MHz, CDCl3); δ 7.21 (d, J=8.3 Hz, 2H), 6.63 (d, J=8.5 Hz, 2H), 5.57 (brs, 1H), 3.66 (s, 2H), 3.58 (s, 3H), 2.48 (m, 4H), 2.02 (m, 1H), 1.80 (m, 1H). LCMS-B: rt 2.35 min; m/z 221.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266864B2
Source datasetuspto-grants-2016_02
ORD IDord-7754872793e845fea06f5ad37ff9d96c
Source noteuspto-grants-2016_02