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HRID 49492作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/49492

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

In analogy to the method described by Gordon W. Gribble, Joseph H. Hoffmann Synthesis 1977, 859-860, the following reaction was performed. 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 one third and poured into 300 ml water. KOH 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US06706751B2
出典データセットuspto-grants-2004_03
ORD IDord-bd86c4538ce548e0b9203acfa8be0660
出典メモuspto-grants-2004_03