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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291565Generated: October 31, 2026

HCID 21278906, compound → 1-[4-(4-Amino-3-methylphenyl)piperazin-1-yl]ethan-1-one

https://huagongshe.com/reaction/2291565

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 21278906HCID 21278906—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1-[4-(4-Amino-3-methylphenyl)piperazin-1-yl]ethan-1-oneHCID 2127891294.8%

Reaction Steps

1-Acetyl-4-(3-methyl-4-nitrophenyl)piperazine (0.5 g) and 5% palladium on carbon (0.1 g) in ethanol (20 ml) were hydrogenated at 60° and 60 p.s.i for 2 hours after which the catalyst was filtered off and the filtrate evaporated. The residue was partitioned between dichloromethane and water, and the aqueous layer extracted two more times with dichloromethane. The combined organic layers yielded 0.42 g of residue (of the title compound) on evaporation. This was recrystallized, m.p. 126°-9° (methanol/ethyl acetate).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04797401
Source datasetuspto-grants-1989_01
ORD IDord-599eea5636c5419c9299f8060f3b3976
Source noteuspto-grants-1989_01