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HRID 41061作成日:2026年10月23日

Iodoethane → 5-Ethoxy-1H-indole

https://huagongshe.com/ja/reaction/41061

反応式

関与物質

役割名称HCID仕込み量
反応物IodoethaneHCID 6340—
反応物Potassium CarbonateHCID 11430—
反応物5-HydroxyindoleHCID 16054—
反応物Dichloromethane methanolHCID 21226129—
溶媒AcetoneHCID 180—
生成物5-Ethoxy-1H-indoleHCID 477766790%

反応条件

温度50 °C

反応手順

A mixture of commercially available 5-hydroxy-indole (18 g, 13.5 mmol), anhydrous K2CO3 (93.5 g, 5 equiv) and iodoethane (40.5 ml, 3.75 equiv) in acetone (180 mL) is stirred at 50° C. under argon. When TLC (dichloromethane-methanol, 95:5) indicates the disappearance of 5-hydroxy-indole (4 days), the mixture is filtered, the solid is washed with acetone, then the filtrate is concentrated to give 17.67 g (90%) of the title compound, which is sufficiently pure to be used in the next step. M.p. 144-146° C. (from ethanol).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530493B2
出典データセットuspto-grants-2013_09
ORD IDord-7954df6899c24f36acc08db5c4700c76
出典メモuspto-grants-2013_09