HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 4-Benzyl-1-methylpiperazin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Benzyl-3-oxopiperazine | HCID 11458177 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Benzyl-1-methylpiperazin-2-one | HCID 13520410 | — |
Reaction Steps
Sodium hydride (50% in oil, 10.4 g., 0.22 mole) is added to a stirred solution of 4-(phenylmethyl)piperazinone (Example 45, 38.0 g., 0.20 mole) in THF (2.0 l.). After 1 hour methyl iodide (80.0 g., 0.75 mole) is added and the reaction solution is refluxed for 2.5 hours. The THF is removed under reduced pressure and the residual oil is partitioned between chloroform and water. Evaporation of the chloroform gives an oil which is chromatographed on silica gel to give the title compound, which is converted to the p-ISA salt, m.p. 138°-140°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04534897 |
| Source dataset | uspto-grants-1985_08 |
| ORD ID | ord-da39e1cce0344da6b27bea2efefbd263 |
| Source note | uspto-grants-1985_08 |