HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1410481Generated: October 30, 2026
p-Fluoronitrobenzene → 1-Methyl-4-(4-nitrophenyl)piperazine
https://huagongshe.com/reaction/1410481
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Methyl-4-(4-nitrophenyl)piperazine | HCID 2825198 | 85.5% |
Reaction Steps
To a solution of 1-methylpiperazine (0.605 m, 5.45 mmol) in DMF (6.25 ml) was added 4-fluoronitrobenzene (0.750 m, 7.07 mmol) and potassium carbonate (1.13 g, 8.18 mmol) and the reaction mixture stirred at 90° C. overnight. The reaction was then cooled to room temperature, diluted with DCM and washed with water. The organic phase was dried over MgSO4 and the solvent removed in vacuo. The residue was purified by silica gel silica chromatography using a 0-10% MeOH in DCM gradient to afford 1-methyl-4-(4-nitrophenyl)piperazine (1.03 g, 4.66 mmol, 85%) as a yellow solid. 1H NMR (DMSO) δ 2.37 (3H, s), 2.58 (4H, t), 3.45 (4H, t), 6.82 (2H, d), 8.12 (2H, d). LCMS (1) Rt: 1.63 min; m/z (ES+) 222.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08921544B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-a3d0fb7a19714b7bbf37b87c9738f451 |
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| Source note | uspto-grants-2014_12 |
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