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HRID 40235作成日:2026年10月25日

Methyl iodide → 5-Bromo-1-methylpyridin-2(1H)-one

https://huagongshe.com/reaction/40235

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物Potassium CarbonateHCID 11430—
反応物5-Bromo-2-hydroxypyridineHCID 599528—
溶媒DimethylformamideHCID 6228—
生成物5-Bromo-1-methylpyridin-2(1H)-oneHCID 13024027—

反応手順

5-Bromopyridin-2(1H)-one (0.250 g, 1.44 mmol) was dissolved in DMF (3 mL) then added iodomethane (0.0943 ml, 1.51 mmol) and potassium carbonate (0.218 g, 1.58 mmol). The reaction was stirred at room temperature overnight. The reaction mixture was concentrated under vacuum. The remaining residue was dissolved in ethyl acetate then washed with water and brine. The aqueous layer was back-extracted with ethyl acetate (3×). The organic layers were combined and dried over sodium sulfate then concentrated under vacuum to afford 5-bromo-1-methylpyridin-2(1H)-one as an orange waxy solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524900B2
出典データセットuspto-grants-2013_09
ORD IDord-d95bd4d1ba5843d38255cf8f6ae40564
出典メモuspto-grants-2013_09