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HRID 78115作成日:2026年10月24日

Dimethylformamide → 5-(Benzyloxy)-2-methylpyridine

https://huagongshe.com/ja/reaction/78115

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Benzyl BromideHCID 7498—
反応物2-Methyl-5-hydroxypyridineHCID 14275—
反応物Sodium hydrideHCID 24758—
溶媒WaterHCID 962—
生成物5-(Benzyloxy)-2-methylpyridineHCID 1239725166%

反応条件

温度0 °C

反応手順

To an N,N-dimethylformamide (50 mL) solution of 3-hydroxy-6-methylpyridine (5.00 g, 45.8 mmol) was added sodium hydride (2.02 g, 50.4 mmol, 60% in oil), which was stirred for 15 minutes at 0° C. Next, benzyl bromide (5.99 mL, 50.4 mmol) was added to this reaction mixture at 0° C., which was stirred for 3.5 hours at room temperature. Water was added to the reaction mixture, which was extracted with ethyl acetate. The organic layer was separated, washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure. The residue was purified by silica gel column chromatography (heptane: ethyl acetate=2:1) to obtain the title compound (5.99 g, 66%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841327B2
出典データセットuspto-grants-2014_09
ORD IDord-9e7c603bc87544609aed79f158418130
出典メモuspto-grants-2014_09