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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1023914생성일: 2026년 10월 26일

Isoamyl Nitrite → 3-Fluoro-2-nitropyridine

https://huagongshe.com/reaction/1023914

반응식

참여 물질

역할이름HCID투입량
반응물Isoamyl NitriteHCID 8053—
반응물Tetrafluoroboric acidHCID 28118—
반응물2-Nitropyridin-3-amineHCID 83281—
용매EthanolHCID 702—
생성물3-Fluoro-2-nitropyridineHCID 276280239%

반응 조건

온도0 °C

반응 단계

To a stirred solution of 3-Amino 2-nitro pyridine (2.5 g, 17.97 mmol) in dry ethanol (20 ml) was added 10 ml of tetrafluoroboric acid (48% in water). The reaction mixture was cooled to 0° C. and isoamyl nitrite (2.6 g, 22.4 mmol) was added dropwise at 0° C. and stirred at 0° C. for 1 hour. The reaction mixture was filtered, and the solid obtained was washed with diethyl ether. The filtered solid was added to preheated (150 mL) toluene with stirring and reaction mixture was refluxed for 24 hours. The solvent was evaporated and the residue taken in ethyl acetate (200 ml) and washed with water followed by brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure to get the crude 3-fluoro-2-nitropyridine. This was purified by column over silica gel using 10% ethyl acetate in pet ether as eluant to get 1 g (39%) of the title compound as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08722746B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-3748984f5eae453bb357fcc69c9f4ec8
출처 메모uspto-grants-2014_05