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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014228Generated: October 31, 2026

Tert-butyl 2-methoxy-5-nitrophenylcarbamate → tert-butyl N-(5-amino-2-methoxyphenyl)carbamate

https://huagongshe.com/reaction/1014228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 2-methoxy-5-nitrophenylcarbamateHCID 45790233—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Producttert-butyl N-(5-amino-2-methoxyphenyl)carbamateHCID 2234474791.6%

Reaction Steps

A solution of 1,1-dimethylethyl [2-(methyloxy)-5-nitrophenyl]carbamate (6 g, 22 mmol) in absolute ethanol (150 mL) was hydrogenated with 10% Pd/C (˜1.00 g, Lancaster) at 50 psi overnight. The catalyst was removed by vacuum filtration through a celite pad, rinsed with methanol, and filtrate was concentrated under reduced pressure to provide 1,1-dimethylethyl [5-amino-2-(methyloxy)phenyl]carbamate (4.8 g, 90%) as a tan solid. ESIMS (M+H)+=239.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981903B2
Source datasetuspto-grants-2011_07
ORD IDord-585c543811e642c08c3fded3ab78aa3e
Source noteuspto-grants-2011_07