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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860403Generated: October 31, 2026

Piperazine → 1-(2-Nitrophenyl)piperazine

https://huagongshe.com/reaction/1860403

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 numberUS06531471B2
Source datasetuspto-grants-2003_03
ORD IDord-97d73d46c93748e496fe8e28f7db246b
Source noteuspto-grants-2003_03