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HRID 10774作成日:2026年10月25日

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

https://huagongshe.com/reaction/10774

反応式

関与物質

役割名称HCID仕込み量
反応物1-MethylpiperazineHCID 53167—
反応物1,2-Difluoro-4-nitrobenzeneHCID 123053—
溶媒AcetonitrileHCID 6342—
生成物1-(2-Fluoro-4-nitrophenyl)-4-methylpiperazineHCID 278305497%

反応手順

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.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07094896B2
出典データセットuspto-grants-2006_08
ORD IDord-7fc712df9bea40238aa90ddb61a7176d
出典メモuspto-grants-2006_08