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HRID 276850作成日:2026年10月26日

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

https://huagongshe.com/reaction/276850

反応式

関与物質

役割名称HCID仕込み量
反応物2-Chloro-5-nitropyridineHCID 78308—
反応物Potassium FluorideHCID 522689—
溶媒Dimethyl SulfoxideHCID 679—
溶媒Ethyl AcetateHCID 8857—
溶媒Sodium chloride; waterHCID 57417360—
生成物2-Fluoro-5-nitropyridineHCID 9526484.8%

反応条件

温度70 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06355636B1
出典データセットuspto-grants-2002_03
ORD IDord-249cdb46c9ec46ec93a04ab666acb7d6
出典メモuspto-grants-2002_03