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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10774Generated: October 25, 2026

1-Methylpiperazine → 1-(2-Fluoro-4-nitrophenyl)-4-methylpiperazine

https://huagongshe.com/reaction/10774

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
Reactant1,2-Difluoro-4-nitrobenzeneHCID 123053—
SolventAcetonitrileHCID 6342—
Product1-(2-Fluoro-4-nitrophenyl)-4-methylpiperazineHCID 278305497%

Reaction Steps

A solution of 3,4-difluoronitrobenzene (12.00 g, 75.4 mmol) (Aldrich) and N-methylpiperazine (18.89 g, 188.6 mmol) in acetonitrile (150 mL) was heated at reflux for 3 h. The reaction mixture was allowed to stand overnight at room temperature, then the solvent was evaporated under reduced pressure and the residue was partitioned between water and ethyl acetate (200 mL each). The aqueous layer was extracted with ethyl acetate (3×200 mL) and the combined organic layers were then washed with water and brine (200 mL each), dried (MgSO4), filtered, and evaporated under reduced pressure to give 1-(2-fluoro-4-nitrophenyl)-4-methylpiperazine as a pale brown solid (17.5 g, 97%, mp 68–70° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094896B2
Source datasetuspto-grants-2006_08
ORD IDord-7fc712df9bea40238aa90ddb61a7176d
Source noteuspto-grants-2006_08