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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2232403Generated: October 31, 2026

1-Acetyl-4-(4-nitrophenyl)piperazine → 1-[4-(4-Aminophenyl)piperazin-1-yl]ethan-1-one

https://huagongshe.com/reaction/2232403

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Acetyl-4-(4-nitrophenyl)piperazineHCID 2865149—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1-[4-(4-Aminophenyl)piperazin-1-yl]ethan-1-oneHCID 73626993.9%

Reaction Steps

A solution of 1-acetyl-4-(4-nitrophenyl)piperazine (28.8 g) in ethanol (400 ml) was hydrogenated at 4 bar in the presence of 10% palladium/carbon (0.5 g) until no further hydrogen was taken up. The catalyst was filtered off and the filtrate was evaporated. The residue was triturated with diethyl ether, filtered and dried to give the title compound (23.8 g), m.p. 142°-144° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04788196
Source datasetuspto-grants-1988_11
ORD IDord-7692e30126f9454f90c0826d46ce0623
Source noteuspto-grants-1988_11