HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Benzylpiperazin-2-one hydrochloride → Tert-butyl 4-benzyl-3-oxopiperazine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Benzylpiperazin-2-one hydrochloride | HCID 12744519 | — |
| Reactant | 2-(t-Butoxycarbonyloxyimino)-2-phenylacetamide | HCID 53719090 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Tert-butyl 4-benzyl-3-oxopiperazine-1-carboxylate | HCID 10891590 | — |
Reaction Steps
A mixture of 1-(phenylmethyl)piperazinone (XIV, Example 40, 19.0 g., 0.1 mole) and 2-(t-butoxycarbonyloxyimino)-2-phenylacetamide (30.0 g., 0.12 mole) in benzene (200 ml.) is heated under reflux for 1 hour. The benzene is removed under reduced pressure, the residual oil is dissolved in ethyl acetate:SSB (1:1) and chromatographed on silica gel. The column is eluted with ethyl acetate, the appropriate fractions are pooled, concentrated and the product is crystallized from ethyl acetate:SSB (1:10) to give the title compound, m.p. 89°-90°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04534897 |
| Source dataset | uspto-grants-1985_08 |
| ORD ID | ord-21d8bf145eaf42c19ca8f0889c9b5263 |
| Source note | uspto-grants-1985_08 |