戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 23403作成日:2026年10月24日

Sodium sulfate decahydrate → 2-(5-chloro-3-methylsulfanyl-1H-indol-2-yl)-ethanol

https://huagongshe.com/ja/reaction/23403

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium sulfate decahydrateHCID 62649—
反応物Aluminium lithium hydrideHCID 21226445—
反応物(5-chloro-3-methylsulfanyl-1H-indol-2-yl)-acetic acid methyl esterHCID 69545956—
溶媒Diethyl EtherHCID 3283—
生成物2-(5-chloro-3-methylsulfanyl-1H-indol-2-yl)-ethanolHCID 22574103—

反応手順

To a solution of (5-chloro-3-methylsulfanyl-1H-indol-2-yl)-acetic acid methyl ester (0.252 g, 0.93 mmole) in ether (10 ml) was added 0.93 ml of a 1M solution of lithium aluminum hydride in ether at room temperature. The reaction mixture was stirred for 15 minutes, after which time sodium sulfate decahydrate (1 g) was cautiously added. The reaction mixture was stirred for an hour at room temperature, filtered, and the filtrate evaporated to dryness. The crude alcohol was purified by column chromatography (silica gel) using 7:3 hexane:ethyl acetate as the eluting solvent. The pure 2-(5-chloro-3-methylsulfanyl-1H-indol-2-yl)-ethanol was isolated as a pale solid (0.191 g, 84% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06852726B2
出典データセットuspto-grants-2005_02
ORD IDord-a4e26d10e9de41e7b1672cfefe6736c6
出典メモuspto-grants-2005_02