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2000
Volume 17, Issue 11
  • ISSN: 1570-1786
  • E-ISSN: 1875-6255

Abstract

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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/content/journals/loc/10.2174/1570178617666200207110109
2020-11-01
2025-09-04
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/content/journals/loc/10.2174/1570178617666200207110109
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  • Article Type:
    Research Article
Keyword(s): 3-Methylindole; Acylation reaction; acylindoles; Amberlyst 15; Friedel-Crafts; ketones
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