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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403614Generated: October 26, 2026

N-bromobutanimide → Benzyl 4-(4-bromophenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2403614

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant1-Piperazinecarboxylic acid, 4-phenyl-, phenylmethyl esterHCID 9879254—
SolventDimethylformamideHCID 6228—
ProductBenzyl 4-(4-bromophenyl)piperazine-1-carboxylateHCID 4673949486.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802679B2
Source datasetuspto-grants-2014_08
ORD IDord-566f931f23a84db8b2e1dbcdd053de75
Source noteuspto-grants-2014_08