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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476561Generated: October 25, 2026

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

https://huagongshe.com/reaction/476561

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Acetyl-4-(4-nitrophenyl)piperazineHCID 2865149—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
Product1-[4-(4-Aminophenyl)piperazin-1-yl]ethan-1-oneHCID 736269—

Reaction Steps

A suspension of 4-acetyl-1-(4-nitrophenyl)piperazine [C. A., 67, P101031Z] (30 g, 0.12 mole) and Raney nickel (2.5 g) in ethanol (500 ml) was hydrogenated at 60 psi (414 kPa) and 40° for 6 hours followed by 18 hours at room temperature. The catalyst was subsequently removed by filtration, the solvent removed under reduced pressure and the residue crystallized from ethyl acetate to yield the title compound, m.p. 129°-130° (18.4 g, 71%), which was used directly in the next stage.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04885294
Source datasetuspto-grants-1989_12
ORD IDord-48c587c122724d43b4582d3b03fd9db0
Source noteuspto-grants-1989_12