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HRID 1409497作成日:2026年10月24日

Dimethylformamide → 2-Fluoro-5-methoxypyridine

https://huagongshe.com/ja/reaction/1409497

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Methyl iodideHCID 6328—
反応物Potassium CarbonateHCID 11430—
反応物6-Fluoropyridin-3-olHCID 2763108—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
溶媒DichloromethaneHCID 6344—
生成物2-Fluoro-5-methoxypyridineHCID 18973109—

反応条件

温度100 °C

反応手順

To a solution of 6-fluoropyridin-3-ol (75 g, 663 mmol) in DMF (265 mL, 663 mmol) were added potassium carbonate (59.7 g, 995 mmol) and iodomethane (108 g, 763 mmol). The resulting slurry was heated at 100° C. for 3 hours. The reaction was diluted with water (1000 mL) and poured into a separatory funnel containing diethyl ether (1000 mL). The layers were separated and the aqueous layer was extracted with diethyl ether (4×500 mL). The combined organic layers were washed with water and then brine, dried over sodium sulfate, filtered and concentrated in vacuo to provide a yellow oil. This oil was diluted with 500 mL of DCM and concentrated to provide a yellow oil with a large amount of an off white precipitate. The mixture was filtered and the derived solid was washed well with DCM. The filtrate was concentrate to provide a mixture consisting of a yellow oil and an off white solid. The solid eas filtered, washing with DCM. Repeat this procedure again and then concentrated the filtrate to provide a yellow oil. The oil was taken up in 100 mL of ether and flashed through a plug of silica gel with 10:1 hexanes:ether to provide 2-fluoro-5-methoxypyridine as a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08921363B2
出典データセットuspto-grants-2014_12
ORD IDord-15434984c59e4d99a0cf261f488716c6
出典メモuspto-grants-2014_12