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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methyl-4-(4-methyl-3-nitrophenyl)piperazine | HCID 58171632 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Cyclohexene | HCID 8079 | — |
| Product | 2-Methyl-5-(4-methylpiperazin-1-yl)benzenamine | HCID 24994140 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08598172B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-8ae15f576e02456c82c4b28391496808 |
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| Source note | uspto-grants-2013_12 |
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