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HRID 506079作成日:2026年10月25日

Ethanol → 6-Iodoindoline

https://huagongshe.com/reaction/506079

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Sodium HydroxideHCID 14798—
反応物1-Acetyl-6-iodoindolineHCID 11666396—
溶媒WaterHCID 962—
生成物6-IodoindolineHCID 1161569664%

反応手順

1-Acetyl-6-iodoindoline (1.06 g, 3.7 mmol), NaOH (1.16 g, 29 mmol), EtOH (8 mL), and H2O (6 mL) are heated at 90° C. overnight. The reaction mixture is then partitioned between H2O and EtOAc. The organic layer is extracted into aqueous HCl. The aqueous layer is in turn basified with NaOH, and is extracted with EtOAc. The organic layer is dried and concentrated. Hexane trituration yields 6-iodoindoline (577 mg, 64%) as a brown solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07781478B2
出典データセットuspto-grants-2010_08
ORD IDord-b285cc92f2814a68946c85edd40a9ab3
出典メモuspto-grants-2010_08