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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10774생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/10774

반응식

참여 물질

역할이름HCID투입량
반응물1-MethylpiperazineHCID 53167—
반응물1,2-Difluoro-4-nitrobenzeneHCID 123053—
용매AcetonitrileHCID 6342—
생성물1-(2-Fluoro-4-nitrophenyl)-4-methylpiperazineHCID 278305497%

반응 단계

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.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094896B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-7fc712df9bea40238aa90ddb61a7176d
출처 메모uspto-grants-2006_08