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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278904Generated: October 27, 2026

Piperazine → 1-(2-Nitrophenyl)piperazine

https://huagongshe.com/reaction/278904

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant1-Bromo-2-nitrobenzeneHCID 11341—
Product1-(2-Nitrophenyl)piperazineHCID 10094992%

Reaction Conditions

Temperature100 °C

Reaction Steps

A heterogenous reaction mixture containing 2-bromo-nitrobenzene (2.02 g, 10.0 mmol) and piperazine (4.3 g, 50.0 mmol) was heated at 100° C. for 10 hours. The orange-red solid was extracted with ethyl acetate and washed thoroughly with 3 N NaOH solution followed by brine. The organic layer was separated and dried over Na2SO4, filtered and the solvent was removed in vacuo. The resulting red oil was purified by column chromatography on silica gel (1:1 hexane/EtOAc followed by 4:1 EtOAc/MeOH) to yield 1-(2-nitrophenyl)-piperazine as an orange-red oil (1.90 g, 92%). It was characterized as a hydrochloride salt. Analysis calculated for C10H14N3O2Cl0.10 CHCl3: C, 47.46; H, 5.56; N, 16.44. Found: C, 47.63; H, 5.69; N. 16.42.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362182B1
Source datasetuspto-grants-2002_03
ORD IDord-292e1c56c9ee4f56b870e2d0e13d33ac
Source noteuspto-grants-2002_03