HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 1-(4-Bromophenyl)-4-methylpiperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(4-Bromophenyl)piperazine | HCID 2735629 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(4-Bromophenyl)-4-methylpiperazine | HCID 11817675 | 73% |
Reaction Steps
1-(4-Bromo-phenyl)-piperazine (19, 4.1 mmol) and potassium carbonate (1.89, 3 eq) in DMF (15 ml) treated with methyl iodide (250 μl, 1.1 equivalents), solution stirred at room temperature overnight. Reaction quenched with deionised water (10 ml), extracted with ethyl acetate. Organic phase washed with sodium hydrogen carbonate to remove any dimethylated impurity, dried and solvent removed to give 1-(4-Bromo-phenyl)-4-methyl-piperazine in 73% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07705027B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-cfc74b61ba60429ead76b4dafd2a0f67 |
| Source note | uspto-grants-2010_04 |