HRID41059

反应详情

EQUATION

反应方程式

HRID 41059 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

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.

WORKUP

后处理

  1. customto come to room temperature
  2. stirringthe mixture is stirred at room temperature for 2 h
  3. extractionIt is then extracted with dichloromethane (4×200 ml)
  4. customthe organic layer is dried
  5. concentrationconcentrated
  6. customThe residue is purified by column chromatography (dichloromethane-methanol, 4:1→methanol-aqueous ammonia 50:1)
  7. customto give crude product (10.18 g, 96%), which
  8. customis crystallized from acetone