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HRID 15050作成日:2026年10月24日

Dimethylformamide → 4-[(E)-2-(4-fluorophenyl)vinyl]-2-(4-methoxybenzyloxy)-pyridine

https://huagongshe.com/ja/reaction/15050

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Potassium CarbonateHCID 11430—
反応物4-FluorostyreneHCID 67883—
反応物4-Iodo-2-((4-methoxybenzyl)oxy)pyridineHCID 66872953—
触媒HCID 178418476HCID 178418476—
溶媒Sodium chloride; waterHCID 57417360—
生成物4-[(E)-2-(4-fluorophenyl)vinyl]-2-(4-methoxybenzyloxy)-pyridineHCID 6687272561%

反応条件

温度100 °C

反応手順

4-Fluorostyrene (3.0 mL), dichlorobis(triphenylphosphine)palladium (870 mg) and potassium carbonate (5.2 g) were added to DMF (70 mL) solution of 4-iodo-2-(4-methoxybenzyloxy)pyridine (4.25 g) and stirred at 100° C. for 19 hours. Saturated brine was added to the reaction liquid, followed by extraction with ethyl acetate and drying over anhydrous magnesium sulfate. Concentrating the solvent under reduced pressure, the resulting residue was purified on silica gel column chromatography (C-200; ethyl acetate:hexane=1:19-1:9-1:4) to provide the title compound (2.55 g, 61%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732456B2
出典データセットuspto-grants-2010_06
ORD IDord-59420ad30a3644888fc89d1d064672b1
出典メモuspto-grants-2010_06