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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1779102Generated: October 31, 2026

Tert-butyl (1-(4-nitrophenyl)ethyl)carbamate → tert-butyl N-[1-(4-aminophenyl)ethyl]carbamate

https://huagongshe.com/reaction/1779102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl (1-(4-nitrophenyl)ethyl)carbamateHCID 57219944—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Producttert-butyl N-[1-(4-aminophenyl)ethyl]carbamateHCID 22569414—

Reaction Steps

A suspension of 10% Pd/C (1.25 g) and tert-butyl (1-(4-nitrophenyl)ethyl)carbamate (A130) (3.78 g, 14.2 mmol) in EtOAc (50 mL) was stirred under a hydrogen atmosphere for 3 hours. The resulting solution was filtered through a pad of Celite, washing with EtOAc, then the filtrate was concentrated in vacuo to give the title compound A131 as a viscous oil (3.01 g, 89%); 1H NMR (300 MHz, CDCl3) δ 7.11 (d, J=8.1 Hz, 2H), 6.70 (d, J=8.0 Hz, 2H), 4.70 (brs, 2H), 1.44 (m, 14H). LCMS-B: 4.444 min; m/z 237 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266864B2
Source datasetuspto-grants-2016_02
ORD IDord-c071fd093e8a42fa8849b9696d85776f
Source noteuspto-grants-2016_02