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HRID 252571作成日:2026年10月25日

Ethanol → 6-Iodoindoline

https://huagongshe.com/reaction/252571

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US07868037B2
出典データセットuspto-grants-2011_01
ORD IDord-a0f13259a14d43c5b16fbd2049ae4af8
出典メモuspto-grants-2011_01