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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907441Generated: October 30, 2026

1-Methyl-4-(4-methyl-3-nitrophenyl)piperazine → 2-Methyl-5-(4-methylpiperazin-1-yl)benzenamine

https://huagongshe.com/reaction/1907441

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Methyl-4-(4-methyl-3-nitrophenyl)piperazineHCID 58171632—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventCyclohexeneHCID 8079—
Product2-Methyl-5-(4-methylpiperazin-1-yl)benzenamineHCID 24994140—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 1-methyl-4-(4-methyl-3-nitro-phenyl)-piperazine (9.0 g, 38.29 mmol) in ethanol (100 mL) and cyclohexene (7 ml), Pd/C 10% (1.5 g) was added. The mixture was heated at 80° C. for 6 hours until HPLC revealed the disappearance of the starting material. The Pd was filtered from the reaction and the solvents were removed from the filtrate under reduced pressure. The crude was diluted with DCM and treated with HCl in dioxane; the precipitate was collected and washed with diethyl ether to give the final compound as a brown solid in quantitative yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598172B2
Source datasetuspto-grants-2013_12
ORD IDord-8ae15f576e02456c82c4b28391496808
Source noteuspto-grants-2013_12