HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromo-2-methylpropane → 1-Methyl-3-(2-methylpropyl)-4-(phenylmethyl)piperazinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromo-2-methylpropane | HCID 6555 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | 4-Benzyl-1-methylpiperazin-2-one | HCID 13520410 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Product | 1-Methyl-3-(2-methylpropyl)-4-(phenylmethyl)piperazinone | HCID 23319687 | — |
Reaction Steps
Butyl lithium (8.0 ml. of 1.6M in hexane, 0.012 mole) is added at -60° to a stirred solution of 1-methyl-4-(phenylmethyl)piperazinone (Example 46, 2.04 g., 0.010 mole), diisopropylamine (1.1 g., 0.011 mole) and hexamethylphosphorotriamide (2.0 ml.) in THF (25 ml.). The solution is allowed to warm to 20°-25°, 1-bromo-2-methylpropane (4.1 g., 0.030 mole) is added and the solution is refluxed for 3 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 dissolved in ethyl acetate and chromatographed on silica gel. Elution of the column with ethyl acetate and pooling of the appropriate fractions gives the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04534897 |
| Source dataset | uspto-grants-1985_08 |
| ORD ID | ord-2ab17d9da9384b4e8b8b8b4a792125e2 |
| Source note | uspto-grants-1985_08 |