戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 41059作成日:2026年10月23日

Dimethylamine → (5-ethoxy-1H-indol-ylmethyl)-dimethyl-amine

https://huagongshe.com/ja/reaction/41059

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylamineHCID 674—
反応物FormaldehydeHCID 712—
反応物Sodium HydroxideHCID 14798—
反応物5-Ethoxy-1H-indoleHCID 4777667—
溶媒Acetic AcidHCID 176—
溶媒Dichloromethane methanolHCID 21226129—
生成物(5-ethoxy-1H-indol-ylmethyl)-dimethyl-amineHCID 6693862296%

反応条件

温度0 °C

反応手順

A mixture of 5-ethoxy-indole (7.84 g, 48.7 mmol), 40% aqueous dimethylamine (9.25 ml, 73 mmol, 1.5 equiv), and 96% acetic acid (30 ml) is stirred at 0° C., then 36% aqueous formaldehyde solution (6.33 ml, 82.7 mmol, 1.7 equiv) is added drop wise. The mixture is allowed to come to room temperature, and after stirring overnight TLC (dichloromethane-methanol, 4:1) indicates the absence of starting material. 10% Aqueous NaOH (150 ml) is added and the mixture is stirred at room temperature for 2 h. It is then extracted with dichloromethane (4×200 ml), the organic layer is dried and concentrated. The residue is purified by column chromatography (dichloromethane-methanol, 4:1→methanol-aqueous ammonia 50:1) to give crude product (10.18 g, 96%), which is crystallized from acetone to provide pure (5-ethoxy-1H-indol-ylmethyl)-dimethyl-amine (10.2 g, 96%) as white crystals. M.p. 95-97° C.

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-389c3916604348d4a7883e4a21a3270a
出典メモuspto-grants-2013_09