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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382651Generated: November 4, 2026

Cesium carbonate → 1-[4-(4-Methoxy-3-nitro-phenyl)-piperazin-1-yl]ethanone

https://huagongshe.com/reaction/2382651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant1-AcetylpiperazineHCID 83795—
Reactant2-(Di-tert-butylphosphino)biphenylHCID 2734215—
Reactant5-Bromo-2-nitroanisoleHCID 11746490—
Catalystpalladium(II) acetateHCID 167845—
Solvent1,4-DioxaneHCID 31275—
Product1-[4-(4-Methoxy-3-nitro-phenyl)-piperazin-1-yl]ethanoneHCID 5823571188.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 5-bromo-1-methoxy-2-nitrobenzene (300 mg, 1.29 mmol) in dioxane, 1-acetyl piperazine (400 mg, 3.12 mmol), cesium carbonate (1.0 g, 3.07 mmol), palladium diacetate (29.0 mg, 0.129 mmol) and 2-(di-t-butylphosphino)biphenyl (77 mg, 0.258 mmol) are added and stirred at 100° C. for 8 hours. After cooling, the mixture is filtered to remove insoluble material. The filtrate is poured into water and extracted with ethyl acetate twice. The organic layer is washed with water and then brine, dried over magnesium sulfate, and evaporated in vacuo. The residue is purified by silica gel column chromatography (n-hexane:ethyl acetate gradient) to afford 1-[4-(4-Methoxy-3-nitro-phenyl)-piperazin-1-yl]-ethanone (319 mg, 44%) as yellow solids.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263590B2
Source datasetuspto-grants-2012_09
ORD IDord-7cae702a0e254384afad4d324ed91369
Source noteuspto-grants-2012_09