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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2189643Generated: October 29, 2026

(4-Tert-butyl-3-nitro-phenyl)-carbamic acid tert-butyl ester → (3-Amino-4-tert-butyl-phenyl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/2189643

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Tert-butyl-3-nitro-phenyl)-carbamic acid tert-butyl esterHCID 66675534—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product(3-Amino-4-tert-butyl-phenyl)-carbamic acid tert-butyl esterHCID 5135818093%

Reaction Steps

A suspension of (4-tert-butyl-3-nitro-phenyl)-carbamic acid tert-butyl ester (3.0 g, 10.19 mol) and 10% Pd—C (1 g) in MeOH (40 mL) was stirred under H2 (1 atm) at room temperature overnight. After filtration, the filtrate was concentrated and the residue was purified by column chromatograph (petroleum ether-EtOAc, 5:1) to give (3-amino-4-tert-butyl-phenyl)-carbamic acid tert-butyl ester (D-10) as a brown oil (2.5 g, 93%). 1H NMR (CDCl3) δ 7.10 (d, J=8.4 Hz, 1H), 6.92 (s, 1H), 6.50-6.53 (m, 1H), 6.36 (s, 1H), 3.62 (br s, 2H), 1.50 (s, 9H), 1.38 (s, 9H); ESI-MS 528.9 m/z (2M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324242B2
Source datasetuspto-grants-2012_12
ORD IDord-891dcfb56fdf45d4ba6d6e36ef4dd2bb
Source noteuspto-grants-2012_12