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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213887Generated: November 2, 2026

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

https://huagongshe.com/reaction/2213887

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Boc-4-(4-Nitrophenyl)piperazineHCID 3380696—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Producttert-Butyl 4-(4-aminophenyl)piperazine-1-carboxylateHCID 1101130199.8%

Reaction Steps

4-(4-Nitrophenyl)-1-piperazinecarboxylic acid, 1,1-dimethylethyl ester (20 g, 65 mmol) was dissolved in anhydrous ethanol (250 mL) and 10% Pd/C (1.8 g) was added. The mixture was stirred for 1.5 h under 10 psi of hydrogen and filtered through a Celite pad. The pad was washed with ethyl acetate (3×100 mL) and the combined solution was evaporated in vacuo to yield 4-(4-amino-phenyl)-1-piperazinecarboxylic acid, 1,1-dimethylethyl ester (18 g, 98% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105670B2
Source datasetuspto-grants-2006_09
ORD IDord-8e4a6e6851894c17880499f9f3ba4931
Source noteuspto-grants-2006_09