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HRID 13286作成日:2026年10月25日

1,4-Dioxane → 2-(2-Fluoro-5-nitrophenyl)pyridine

https://huagongshe.com/reaction/13286

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-DioxaneHCID 31275—
反応物2-Bromo-1-fluoro-4-nitrobenzeneHCID 69699—
反応物Sodium BicarbonateHCID 516892—
生成物2-(2-Fluoro-5-nitrophenyl)pyridineHCID 22285300—

反応手順

0.55 g of Tetrakis-triphenylphosphine palladium was added to a 1,4-dioxane (20 ml) solution of 2.1 g of 3-bromo-4-fluoro-nitrobenzene and 2.3 g of 2-trimethyltin-pyridine, and the reaction liquid was heated overnight under reflux. Aqueous saturated sodium bicarbonate was added to the reaction liquid, and extracted with ethyl acetate. The organic layer was washed with water and saturated saline, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure, and the resulting residue was purified through silica gel column chromatography (developing solvent: hexane/ethyl acetate=7/1) to obtain the entitled compound as a yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728025B2
出典データセットuspto-grants-2010_06
ORD IDord-b06ca7ffde7348cc9499a39a52f86f8f
出典メモuspto-grants-2010_06