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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1390987Generated: October 31, 2026

1-Methyl-4-(4-nitrobenzyl)piperazine → 4-((4-Methylpiperazin-1-yl)methyl)aniline

https://huagongshe.com/reaction/1390987

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Methyl-4-(4-nitrobenzyl)piperazineHCID 677795—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product4-((4-Methylpiperazin-1-yl)methyl)anilineHCID 315399630%

Reaction Steps

A suspension of 1-[(4-nitrophenyl)methyl]-4-methylpiperazine (3.5 g, 0.015 M) and 700 mg of 5% Pd/C in 200 ml of absolute ethanol is hydrogenated for 20 minutes. This is then filtered, washed with more ethanol and concentrated to a white oil. This is crystallized from acetate/Skellysolve® B to give 900 mg (30%) of white crystalline 1-methyl-4-[(4-aminophenyl)methyl]piperazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04140775
Source datasetuspto-grants-1979_02
ORD IDord-0695f04e803d4533abb64949b4deddcc
Source noteuspto-grants-1979_02