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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066979Generated: October 30, 2026

Piperazine → 1-(2-Nitrophenyl)piperazine

https://huagongshe.com/reaction/1066979

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-1-nitrobenzene (2.02 g, 10.0 mmol) and piperazine (4.3 g, 50.0 mmol) was heated at 100° C. for 10 h. 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 converted to its hydrochloride salt. Anal. calcd. for C10H14N3O2Cl.0.10 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 numberUS06245773B1
Source datasetuspto-grants-2001_06
ORD IDord-84b74ddc0ee24a33bbee343ebb2f096e
Source noteuspto-grants-2001_06