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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176866Generated: November 1, 2026

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

https://huagongshe.com/reaction/2176866

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-nitrobenzeneHCID 11466—
Reactant1-EthylpiperazineHCID 79196—
SolventWaterHCID 962—
SolventDichloromethane methanolHCID 21226129—
Product1-Ethyl-4-(4-nitrophenyl)piperazineHCID 285754988.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 1-bromo-4-nitrobenzene (6 g, 29.7 mmol) and 1-ethylpiperazine (7.6 ml, 59.4 mmol, 2 eq.) is heated to 80° C. for 15 h. After cooling to RT, the reaction mixture is diluted with water and DCM/MeOH, 9:1. The aqueous layer is separated and extracted with DCM/MeOH, 9:1. The organic phase is washed with brine, dried (sodium sulfate), filtered and concentrated. Purification of the residue by silica gel column chromatography (DCM/MeOH+1% NH3aq, 9:1) affords 6.2 g of the title compound as a yellow solid: ESI-MS: 236.0 [MH]+; tR=2.35 min (purity: 100%, gradient J); TLC: Rf=0.50 (DCM/MeOH+1% NH3aq, 9:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067896B2
Source datasetuspto-grants-2015_06
ORD IDord-a788ed81e8804b7eaa758a8050919dcd
Source noteuspto-grants-2015_06