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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728812Generated: October 30, 2026

p-Fluoronitrobenzene → 1-Benzyl-4-(4-nitrophenyl)piperazine

https://huagongshe.com/reaction/728812

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-FluoronitrobenzeneHCID 9590—
ReactantPotassium CarbonateHCID 11430—
Reactant1-BenzylpiperazineHCID 75994—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
Product1-Benzyl-4-(4-nitrophenyl)piperazineHCID 2747427—

Reaction Steps

Reflux a mixture of 53.5 mL (0.504 mol) of 1-fluoro-4-nitrobenzene, 99.14 g(0.555 mol) of 1-benzylpiperazine, and 76.7 g (0.555 mol) potassium carbonate in acetonitrile for about 17 h. Cool the mixture to room temperature and dilute with methylene chloride and filter. Concentrate thefiltrate in vacuo. Dissolve the residue in methylene chloride and wash withwater. Dry the organic layer with anhydrous sodium sulfate and concentrate in vacuo to give the title compound. NMR (DMSO-d6): δ=2.59(t,4),3.42(t,4), 3.57(s,2), 6.80(d,2) 7.34(m,5) and 8.11(d,2) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05051423
Source datasetuspto-grants-1991_09
ORD IDord-825d4406ae1e4fd48ff47cfccaa05e6e
Source noteuspto-grants-1991_09