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HRID 3385作成日:2026年10月24日

Benzyl Bromide → 1H-Indol-5-ol, 1-(phenylmethyl)-

https://huagongshe.com/ja/reaction/3385

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5-MethoxyindoleHCID 13872—
反応物Sodium hydrideHCID 24758—
反応物Boron tribromide dichloromethaneHCID 22277759—
溶媒DichloromethaneHCID 6344—
生成物1H-Indol-5-ol, 1-(phenylmethyl)-HCID 1077546219%

反応条件

温度-5 °C

反応手順

5-Methoxy-1H-indole (5.6 g, 21.5 mmol) was reacted with 1.0 g (25 mmol) of 60% sodium hydride and then 3.0 mL (25 mmol) of benzyl bromide by the method described in Example 12, Part D to give crude 5-methoxy-1-(phenylmethyl)-1H-indole. This material was dissolved in 250 mL of methylene chloride, cooled to -5° C., 50 mL of 1M BBr3 /CH2Cl2 added, the cooling bath removed and the mixture stirred for 1.75 hours. Ice water was added and the mixture stirred. The organic layer was separated, washed with saturated NaCl, dried (Na2 SO4), and concentrated at reduced pressure. The residue was chromatographed on silica gel and eluted with 20% ether/hexane→ether to give 870 mg (19% overall yield) of crude 5-hydroxy-1-(phenylmethyl)-1H-indole.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05733923
出典データセットuspto-grants-1998_03
ORD IDord-39e0ce5ac6fe453c825a8e16562f634e
出典メモuspto-grants-1998_03