HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → Benzyl 4-(4-bromophenyl)piperazine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 1-Piperazinecarboxylic acid, 4-phenyl-, phenylmethyl ester | HCID 9879254 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Benzyl 4-(4-bromophenyl)piperazine-1-carboxylate | HCID 46739494 | 86.5% |
Reaction Steps
Benzyl 4-phenylpiperazine-1-carboxylate (2.1 g) was dissolved in DMF (80 ml), and N-bromosuccinimide (1.4 g) was added thereto, followed by stirring at room temperature for 2 hours. The reaction mixture was concentrated under reduced pressure and subjected to liquid separation by the addition of CHCl3 and a saturated aqueous sodium hydrogen carbonate solution. The organic layer was separated and dried over Na2SO4, and then the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/EtOAc) to obtain benzyl 4-(4-bromophenyl)piperazine-1-carboxylate (2.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08802679B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-566f931f23a84db8b2e1dbcdd053de75 |
| Source note | uspto-grants-2014_08 |