HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 549403Generated: October 29, 2026
Methyl iodide → 3-(4-Bromo-phenyl)-1-methyl-piperazine
https://huagongshe.com/reaction/549403
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-(4-Bromophenyl)piperazine | HCID 21838686 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3-(4-Bromo-phenyl)-1-methyl-piperazine | HCID 57899227 | 46.3% |
Reaction Steps
To a cooled (0° C.) solution of 2-(4-bromophenyl)piperazine (4.07 g, 16.0 mmol) and triethylamine (17 mL, 122 mmol) in acetone (50 mL) was added a solution of methyl iodide (1.4 mL, 22 mmol) in acetone (20 mL) over 50 min and the reaction mixture was stirred at 0° C. for 15 minutes, warmed to room temperature, and stirred for 16 h. The reaction mixture was slowly treated with saturated ammonium chloride (150 mL) and extracted with ethyl acetate (200 mL×3). The organic layers were combined, dried over magnesium sulfate, filtered and concentrated in vacuo. Purification via flash silica gel column chromatography (heptane/ethyl acetate) gave 3-(4-bromo-phenyl)-1-methyl-piperazine (1.89 g, 46% yield). LCMS (m/z): 257.00 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07943652B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-bc8f167e016942a4a35010e6b8e2f49a |
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| Source note | uspto-grants-2011_05 |
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