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HRID 430773作成日:2026年10月25日

Benzyl Bromide → 4-(phenylmethoxy)-1H-indole

https://huagongshe.com/reaction/430773

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl BromideHCID 7498—
反応物Potassium HydroxideHCID 14797—
反応物1H-indol-4-olHCID 75421—
溶媒DimethylformamideHCID 6228—
生成物4-(phenylmethoxy)-1H-indoleHCID 8846585%

反応手順

Potassium hydroxide (0.42 g) was added to 4-hydroxyindole (1.00 g) in DMF (25 ml), and the solution was stirred at room temperature for 15 minutes. Benzyl bromide (1.00 ml) was added to the solution, and the solution was stirred at room temperature for 1.5 hours. Since the reaction was not completed, benzyl bromide (0.20 ml) was further added and the solution was stirred for 5 hours. After removing the solvent under reduced pressure, water (50 ml) was added to the residue and the resultant was extracted with ether (3×50 ml). The organic layers were washed with saturated brine, and dried over sodium sulfate. After removing solids by filtration, the solvent was removed under reduced pressure and the obtained crude product was purified by silica gel column chromatography to obtain the desired product (1.43 g, yield: 85%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06323235B1
出典データセットuspto-grants-2001_11
ORD IDord-ded0112ca83f4afa952d72e5c70ce665
出典メモuspto-grants-2001_11