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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1187129Generated: October 30, 2026

Ammonium Chloride → 1-(4-Nitrophenyl)-2-{4-[2-(4-nitrophenyl)ethyl]piperazin-1-yl}ethanone

https://huagongshe.com/reaction/1187129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Bromo-4'-nitroacetophenoneHCID 66840—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-[2-(4-Nitrophenyl)ethyl]piperazine hydrochlorideHCID 66644006—
Product1-(4-Nitrophenyl)-2-{4-[2-(4-nitrophenyl)ethyl]piperazin-1-yl}ethanoneHCID 49801326—

Reaction Steps

2-Bromo-1-(4-nitrophenyl)ethanone (269 mg, 1.10 mmol) was added to a stirred solution of 1-[2-(4-nitrophenyl)ethyl]piperazine hydrochloride (200 mg, 0.736 mmol) followed by Hünig's base, then was stirred at RT for 1 h. The reaction mixture was poured into saturated NH4Cl solution and extracted twice with ethyl acetate. The combined organic layers were washed with water, then brine. The organic layer was dried over MgSO4, filtered, and concentrated. The residue was purified by preparative TLC using 5% MeOH/DCM solvent system to yield 1-(4-nitrophenyl)-2-{4-[2-(4-nitrophenyl)ethyl]piperazin-1-yl}ethanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673920B2
Source datasetuspto-grants-2014_03
ORD IDord-bd3b112d6e0a4907ba2ebff8f5ff8d94
Source noteuspto-grants-2014_03