HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methylpiperazine → 1-(4-Fluorobenzyl)-3-methylpiperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methylpiperazine | HCID 66057 | — |
| Reactant | 4-Fluorobenzyl bromide | HCID 68021 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(4-Fluorobenzyl)-3-methylpiperazine | HCID 10703584 | 12% |
Reaction Steps
To a solution of 2-methylpiperazine (0.10 g, 1 mmol) in CH2Cl2 (2 mL) was added 4-fluorobenzyl bromide (0.125 mL, 1 mmol). The resultant mixture was stirred at ambient temperature. After 15 hours, the mixture was concentrated in vacuo to afford a solid. This solid was dissolved in CH2Cl2 and washed sequentially with water, aqueous NaHCO3 solution, then brine. The organic layer was dried over MgSO4, filtered, and concentrated to an oil. Purification by flash column chromatography afforded 0.025 g (12% yield) of 1-(4-fluorobenzyl)-3-methylpiperazine, a compound of formula (C), as a colorless oil; NMR (CDCl3) 7.3 (m, 2), 7.0 (m, 2), 3.4 (s, 2), 3.0-2.6 (m, 5), 2.0 (br s, 2), 1.6 (t, 1), 1.0 (d, 3) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06541476B1 |
| Source dataset | uspto-grants-2003_04 |
| ORD ID | ord-1949a0e806c34fea906a047e0f622508 |
| Source note | uspto-grants-2003_04 |