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HRID 473423作成日:2026年10月27日

Water → 5-Fluoro-3-nitro-2-vinylpyridine

https://huagongshe.com/reaction/473423

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物TributylvinyltinHCID 81998—
反応物2-Bromo-5-fluoro-3-nitropyridineHCID 20791243—
触媒Dichlorobis(triphenylphosphine)palladiumHCID 6102075—
溶媒1,4-DioxaneHCID 31275—
生成物5-Fluoro-3-nitro-2-vinylpyridineHCID 58318638—

反応条件

温度110 °C

反応手順

To a solution of 2-bromo-5-fluoro-3-nitropyridine (20 g, 90.50 mmol) in 1, 4 dioxane (270 mL) was added tributyl vinyl tin (34.54 g, 108.60 mmol). The reaction mixture was degassed using nitrogen for 30 min. Bis-(triphenylphosphin)-palladium(II)-chloride (3.17 g, 4.5 mmol) was added to the reaction mixture. Reaction mass was stirred at 110° C. for 16 h. The reaction mixture was cooled to 25° C. Water was added to the reaction mass and extracted with EtOAc. Organic layer was washed with brine and dried over Na2SO4. The organic layer was concentrated in vacuo and purified by column chromatography on silica gel using 0-2% EtOAc in hexane to give 5-fluoro-3-nitro-2-vinylpyridine: 1H NMR (400 MHz, DMSO-d6): δ 5.742 (dd, 1H, J=2 Hz, 10.8 Hz), 6.45 (dd, 1H, J=2 Hz, J=16.8 Hz), 7.11-7.17 (m, 1H), 8.489-8.516 (m, 1H), 8.959 (d, 1H, J=2.4 Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08633313B2
出典データセットuspto-grants-2014_01
ORD IDord-251d108115194ba7a6729f7cd7b6c1b3
出典メモuspto-grants-2014_01