Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228071Generated: October 29, 2026

1-Boc-4-(2-nitrophenyl)piperazine → tert-Butyl 4-(2-aminophenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/228071

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Boc-4-(2-nitrophenyl)piperazineHCID 21935210—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Producttert-Butyl 4-(2-aminophenyl)piperazine-1-carboxylateHCID 279553099.1%

Reaction Steps

Into a 500 mL round bottomed flask equipped with magnetic stirring was added tert-butyl 4-(2-nitrophenyl)piperazinecarboxylate (5.0 g, 16 mmol) in 95% EtOH (250 mL), and 10% Pd/C (2.0 g, 1.9 mmol) (Aldrich). The flask was equipped with a balloon filled with H2, and the reaction was stirred for 18 h. After filtering through a pad of Celite®, the crude material was concentrated in vacuo to afford the desired compound (4.4 g). MS (ESI, pos. ion) m/z: 278 (M+H), (ESI, neg. ion) m/z: 276 (M−H). Calc'd for C15H23N3O2: 277.18.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560460B2
Source datasetuspto-grants-2009_07
ORD IDord-64006f00f32e4129a46544abc1a97b85
Source noteuspto-grants-2009_07