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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213879Generated: October 30, 2026

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

https://huagongshe.com/reaction/2213879

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 numberUS07105670B2
Source datasetuspto-grants-2006_09
ORD IDord-cd37b54722f54e7382164544c43313f5
Source noteuspto-grants-2006_09