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Synthesis of N‐Heteroaryl(trifluoromethyl)hydroxyalkanoic Acid Esters by Highly Efficient Solid Acid‐Catalyzed Hydroxyalkylation of Indoles and Pyrroles with Activated Trifluoromethyl Ketones
Author(s) -
Abid Mohammed,
Török Béla
Publication year - 2005
Publication title -
advanced synthesis and catalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.541
H-Index - 155
eISSN - 1615-4169
pISSN - 1615-4150
DOI - 10.1002/adsc.200505117
Subject(s) - chemistry , trifluoromethyl , catalysis , yield (engineering) , organic chemistry , montmorillonite , selectivity , friedel–crafts reaction , combinatorial chemistry , alkyl , materials science , metallurgy
The synthesis of N‐heteroaryl(trifluoromethyl)hydroxyalkanoic acid esters by solid acid‐catalyzed Friedel–Crafts hydroxyalkylation of indoles and pyrroles with ethyl 3,3,3‐trifluoropyruvate and ethyl 4,4,4‐trifluoroacetoacetate is described. The inexpensive and readily available K‐10 montmorillonite is found to be an efficient catalyst for the synthesis of a wide variety of trifluoromethylated indol‐3‐yl‐ and pyrrol‐2‐yl‐hydroxypropionic and ‐butanoic acid esters. Using a series of substituted indoles and pyrroles the corresponding products were isolated in excellent yield (up to 98%) and 100% selectivity under mild experimental conditions, during very short reaction times. Beyond these, the ease of product isolation, catalyst stability and handling make this process an attractive, environmentally benign alternative for the synthesis of the target compounds.