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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353713Generated: October 27, 2026

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

https://huagongshe.com/reaction/353713

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 numberUS06756374B2
Source datasetuspto-grants-2004_06
ORD IDord-c9555bd78b9a42b0970bc9afb83aade3
Source noteuspto-grants-2004_06