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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 557728Generated: October 26, 2026

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

https://huagongshe.com/reaction/557728

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Boc-4-(4-Nitrophenyl)piperazineHCID 3380696—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl 4-(4-aminophenyl)piperazine-1-carboxylateHCID 11011301—

Reaction Steps

A mixture of 4-(4-nitro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester (3 g, 9.76 mmol) and 10% palladium on carbon (300 mg) in 50 mL ethanol and 20 mL ethyl acetate was hydrogenated at room temperature under a 50 psi hydrogen atmosphere for 2 hrs. The reaction mixture was filtered through a plug of Celite and evaporated under reduced pressure to give 4-(4-amino-phenyl)-piperazine-1-carboxylic acid tert-butyl ester that was used in the in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058299B2
Source datasetuspto-grants-2011_11
ORD IDord-5754f8080df0404192c7a5848b49076d
Source noteuspto-grants-2011_11