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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409672Generated: October 26, 2026

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

https://huagongshe.com/reaction/409672

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 numberUS08759517B2
Source datasetuspto-grants-2014_06
ORD IDord-58bd338a40824640897be00271babb1d
Source noteuspto-grants-2014_06