化学
催化作用
弗里德尔-克拉夫茨反应
选择性
酰化
有机化学
反应条件
离子交换树脂
作者
Darío A. Vargas,Leticia J. Méndez,Alicia S. Cánepa
标识
DOI:10.2174/1570178617666200207110109
摘要
A simple and efficient methodology for Friedel-Crafts acylation of 3-methylindole using Amberlyst 15 resin as catalyst is described. This methodology shows good selectivity towards the formation of the products of 2-acylation, (3-methyl-1H-indol-2-yl)ketones. Several advantages can be ascribed to Amberlyst 15, among them; are the ease of handling, quick separation from the reaction mixture and minimum or no production of the chemical residues that must be eliminated. Besides, the catalyst can be easily recycled and reused with a minimal loss in activity through 6 reaction cycles. The catalyst was characterized by FT-IR spectroscopy and superficial acidity.
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