HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907440Generated: November 2, 2026
1-Methylpiperazine → 1-Methyl-4-(4-methyl-3-nitrophenyl)piperazine
https://huagongshe.com/reaction/1907440
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 4-Fluoro-2-nitrotoluene | HCID 67965 | — |
| Product | 1-Methyl-4-(4-methyl-3-nitrophenyl)piperazine | HCID 58171632 | 48.3% |
Reaction Steps
In a cylindrical quartz tube were placed 4-fluoro-1-methyl-2-nitro-benzene (20.0 g, 129 mmol) and N-methyl-piperazine (26 g, 258 mmol). The reaction was heated for 48 hours at 200° C. until HPLC revealed the disappearance of the starting material. The solvent was removed under reduced pressure and the residue was dissolved in DCM. The solution was washed twice with water and the organic phase was dried over anhydrous Na2SO4 and the solvent was removed under reduced pressure. The final compound (14.65 g, 48% yield) was obtained as a brown oil.
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-a93557995aac4e9bacc2228476afc19f |
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| Source note | uspto-grants-2013_12 |
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