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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 751591Generated: October 30, 2026

Ethanol → tert-Butyl 4-(4-aminophenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/751591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant1-Boc-4-(4-Nitrophenyl)piperazineHCID 3380696—
CatalystPalladiumHCID 23938—
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 (11) (18.9 mmol), 10% palladium-on-carbon (600 mg), ethanol (100 mL), and ethyl acetate (100 mL) is hydrogenated at room temperature and 40 psi for 2 hrs. The mixture is filtered through celite, washing with ethyl acetate (2×100 mL), and concentrated in vacuo to give 4-(4-amino-phenyl)-piperazine-1-carboxylic acid tert-butyl ester (12) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07405295B2
Source datasetuspto-grants-2008_07
ORD IDord-0e6449432c9f48c2880418c23795164b
Source noteuspto-grants-2008_07