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HRID 276850생성일: 2026년 10월 26일

2-Chloro-5-nitropyridine → 2-Fluoro-5-nitropyridine

https://huagongshe.com/reaction/276850

반응식

참여 물질

역할이름HCID투입량
반응물2-Chloro-5-nitropyridineHCID 78308—
반응물Potassium FluorideHCID 522689—
용매Dimethyl SulfoxideHCID 679—
용매Ethyl AcetateHCID 8857—
용매Sodium chloride; waterHCID 57417360—
생성물2-Fluoro-5-nitropyridineHCID 9526484.8%

반응 조건

온도70 °C

반응 단계

To 100 g of 2-chloro-5-nitropyridine (Aldrich) in 600 mL of dimethyl sulfoxide under an inert atmosphere was added 100 g of anhydrous KF. The reaction was heated at 70° C. for 18 hours before cooling and diluting with 500 mL each of brine, ethyl acetate, and hexanes. This mixture was filtered through a pad of celite, the organic phase was separated, and the aqueous phase was extracted three times with equal volumes of ethyl acetate and hexanes. The pooled organic phases were washed with brine, dried with anhydrous sodium sulfate, and stripped of the solvents. This crude product was passed through a plug of silica gel with a gradient of 10-30% ethyl acetate/hexanes and stripped to constant weight on a rotary evaporator to give 76 g (84%) of 2-fluoro-5-nitropyridine as an oil, which was used in the following procedure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06355636B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-249cdb46c9ec46ec93a04ab666acb7d6
출처 메모uspto-grants-2002_03