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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2278832Generated: November 1, 2026

Piperazine → 1-(4-Nitrophenyl)piperazine

https://huagongshe.com/reaction/2278832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant1-Bromo-4-nitrobenzeneHCID 11466—
ReactantPotassium Phosphate, TribasicHCID 62657—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventIsopropanolHCID 3776—
Product1-(4-Nitrophenyl)piperazineHCID 8044749.4%

Reaction Steps

8.10 g p-nitro-bromobenzene was added into a 250 ml round-bottom flask containing 50 mL isopropanol, then 7.00 g anhydrous piperazine, 15.00 g anhydrous K3PO4 and 4 ml glycol was added, then 2.00 g CuI was added as catalyster under nitrogen atmosphere (the small-scale reaction was carried out in the absence of nitrogen atmosphere, the results showed mat the yield was low probably because of the oxidation of CuI). The reaction mixture was refluxed for two days under nitrogen atmosphere. The crude product was filtered and concentrated. The concentrate was extracted with chloroform/water. The chloroform extract was dried by anhydrous Na2SO4. Based on higher polarity of product and lower polarity of the starting material, the extract was purified by column-chromatography with gradient elution of petroleum ether:ethyl acetate:ethanol in differ ratio, concentrated the eluate, to produce N-4-nitro-phenyl piperazine as yellow solid (4.10 g, 49.4% yield). Mp: 126-128° C. (lit.: 130-132° C.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133195B2
Source datasetuspto-grants-2015_09
ORD IDord-075793d646804c5296524f22ebb697b6
Source noteuspto-grants-2015_09