10601-19-1
10601-19-1 结构式
基本信息
5-甲氧基吲哚-3-醛
5-甲氧基吲哚-3-羧酸
5-甲氧基-3-甲酰基吲哚
5-METHOXY-1H-INDOLE-3-CARBALDEHYDE
5-METHOXY-1H-INDOLE-3-CARBOXALDEHYDE
5-METHOXY-3-FORMYLINDOLE
5-METHOXY-3-INDOLECARBALDEHYDE
5-METHOXY-3-INDOLECARBOXALDEHYDE
5-METHOXYINDOLE-3-ALDEHYDE
5-METHOXYINDOLE-3-CARBALDEHYDE
5-METHOXYINDOLE-3-CARBOXALDEHYDE
5-METHOXYINDOLE-3-CARBOXYALDEHYDE
5-METHOXYINDOLYL-3-ALDEHYDE
5-METHOXYLINDOLE-3-CARBOXALDEHYDE
AKOS JY2083388
5-methoxyindole-3-formaldehyde
5-METHOXYINDOLE-3-CARBOXALDEHYDE, 99+%
5-Methoxyindole-3-CarboxalDehyde(ForTegaserodMaleate)
5-Methoxyindole-3-Carboxaldehyde98%
5-Methoxyindole-3-Carboxaladehyde
5-Methoxyindole-3-Cabroxaldehyde
5-Methoxyindole-3-Carboxaldehyde 98%
物理化学性质
安全数据
制备方法
1006-94-6
68-12-2
10601-19-1
一般步骤:在冰浴冷却下,将草酰氯(0.3 mL)逐滴加入搅拌中的N,N-二甲基甲酰胺(DMF,3 mL)中。反应混合物在0℃下持续搅拌1小时。随后,将5-甲氧基吲哚(4 mmol)溶于DMF(1.5 mL)的溶液逐滴加入上述混合物中。所得混合物在室温下搅拌5小时。反应完成后,加入2 N氢氧化钠溶液(2 mL),并将混合物加热至100℃维持10分钟。反应液冷却后,用乙酸乙酯(3×50 mL)进行萃取。合并有机相,依次用水和饱和食盐水洗涤。有机层经无水硫酸钠干燥后,减压浓缩得到粗产物。粗产物通过快速柱色谱法纯化,洗脱剂为乙酸乙酯/石油醚(3:1,v/v),最终得到纯的5-甲氧基吲哚-3-甲醛。
参考文献:
[1] Organic Letters, 2013, vol. 15, # 11, p. 2636 - 2639
[2] Chinese Chemical Letters, 2010, vol. 21, # 11, p. 1307 - 1309
[3] Synthetic Communications, 1988, vol. 18, # 7, p. 671 - 674
[4] European Journal of Medicinal Chemistry, 2013, vol. 65, p. 158 - 167
[5] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1993, # 21, p. 2561 - 2566
