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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2066702Generated: November 3, 2026

1-Bromo-4-nitrobenzene → 1-Benzyl-4-(4-nitrophenyl)piperazine

https://huagongshe.com/reaction/2066702

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-nitrobenzeneHCID 11466—
Reactant1-BenzylpiperazineHCID 75994—
SolventWater methylene chlorideHCID 21908982—
Product1-Benzyl-4-(4-nitrophenyl)piperazineHCID 2747427—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 1-bromo-4-nitrobenzene (5 g, 24.8 mmol) and 1-benzylpiperazine (8.6 ml, 49.5 mmol, 2 equiv) is heated to 80° C. for 17 h. The reaction mixture is allowed to cool to RT, and is diluted with DCM/H2O. The layers are separated and the aqueous phase is extracted with DCM. The combined organic phase is washed with brine, dried (Na2SO4), filtered and concentrated. Purification of the residue by silica gel column chromatography (Hex/EtOAc, 1:1) affords the title compound as a yellow solid: ESI-MS: 298.3 [MH]+; tR=3.25 min (purity: 100%, system 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293746B2
Source datasetuspto-grants-2012_10
ORD IDord-9d26fdaa653542c887cc1ef7d056b419
Source noteuspto-grants-2012_10