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HRID 1633673作成日:2026年10月26日

Water → 5-(Benzyloxy)-2,3-dihydro-1H-indole

https://huagongshe.com/reaction/1633673

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物5-BenzyloxyindoleHCID 14624—
反応物Potassium HydroxideHCID 14797—
反応物Sodium cyanoborohydrideHCID 5003444—
溶媒Acetic AcidHCID 176—
生成物5-(Benzyloxy)-2,3-dihydro-1H-indoleHCID 1679488189.2%

反応手順

This example was carried out in analogy to: Gordon W. Gribble, Joseph H. Hoffmann Synthesis 1977, 859-860. To a precooled solution of 22.3 g (0.1 mol) 5-benzyloxyindole in 270 ml acetic acid, 19 g (0.3 mol) NaCNBH3 were added. The solution was stirred at RT for 2 h, the volume was reduced to a third and poured into 300 ml water. Potassium hydroxide was added under cooling, and the solution was extracted with ether. The combined organic phases were washed with water, dried over Na2SO4 and evaporated to yield 20.1 g (89%) 5-Benzyloxy-2,3-dihydro-1H-indole as colorless oil, MS: 225 (M).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06503907B2
出典データセットuspto-grants-2003_01
ORD IDord-d87fea5eadef4b14ba1f76e9e3fd3b46
出典メモuspto-grants-2003_01