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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1261981Generated: October 28, 2026

Methanol → (4-Aminophenyl)(4-methylpiperazin-1-yl)methanone

https://huagongshe.com/reaction/1261981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant(4-Methylpiperazin-1-yl)(4-nitrophenyl)methanoneHCID 716396—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
Product(4-Aminophenyl)(4-methylpiperazin-1-yl)methanoneHCID 23140899.7%

Reaction Steps

(4-Methyl-piperazin-1-yl)-(4-nitro-phenyl)-methanone (2.12 g, 8.51 mmol) was dissolved in Methanol (35 mL, 860 mmol) and the solution was carefully added to a Parr vessel containing 10% Palladium on Carbon (0.650 g, 48.7 mmol) under nitrogen. The mixture was then placed on a Parr hydrogenation apparatus and was allowed to shake at 55 psi until uptake of hydrogen ceased. The catalyst was then filtered to afford 1.86 g of (4-Amino-phenyl)-(4-methyl-piperazin-1-yl)-methanone without further purification. (M+H)=220.6. 1H NMR (400 MHz, DMSO, d6) δ 7.09 (d, 2H, J=8.41 Hz), 6.53 (d, 2H J=8.41 Hz), 5.48 (s, 2H), 3.46 (m, 4H), 2.28 (m, 4H), 2.17 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08471005B2
Source datasetuspto-grants-2013_06
ORD IDord-733c82cdc92d4bc4a9b42801109bae0a
Source noteuspto-grants-2013_06