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HRID 907179作成日:2026年10月25日

Ethanol → 6-Iodoindoline

https://huagongshe.com/reaction/907179

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) were heated at 90° C. overnight. The reaction mixture was then partitioned between H2O and EtOAc. The organic layer was extracted into aqueous HCl. The aqueous layer was in turn basified with NaOH, and was extracted with EtOAc. The organic layer was dried and concentrated. Hexane trituration yielded 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US08013006B2
出典データセットuspto-grants-2011_09
ORD IDord-0ec4d54cb95b4cc78d773166451d5bb4
出典メモuspto-grants-2011_09