A Kinetic Study of the Step of Aryl Halide Activation in a Direct Arylation Reaction of Indole under Real Catalysis Conditions
- Authors: Larina E.V.1, Yarosh E.V.1, Lagoda N.A.1, Kurokhtina A.A.1, Schmidt A.F.1
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Affiliations:
- Faculty of Chemistry, Irkutsk State University
- Issue: Vol 60, No 3 (2019)
- Pages: 337-342
- Section: Article
- URL: https://journal-vniispk.ru/0023-1584/article/view/164251
- DOI: https://doi.org/10.1134/S0023158419030091
- ID: 164251
Cite item
Abstract
This paper presents the results of a kinetic study on the step of activation of aryl iodides and aryl bromides under conditions of ligand-free catalysis in the direct arylation of indole at a C–H bond performed using an analysis of the integral kinetic curves of consumption of the competing aryl halides. In the course of an experiment under the conditions of competition between a pair of aryl halides having different reactivity, an acceleration in the consumption of a less active substrate was observed, which coincided in time with the almost complete consumption of a more active one. The experimental data unambiguously indicated a rapid character of the stage of oxidative addition with the participation of not only reactive aryl iodides but also nonactivated aryl bromides.
About the authors
E. V. Larina
Faculty of Chemistry, Irkutsk State University
Email: aschmidt@chem.isu.ru
Russian Federation, Irkutsk, 664033
E. V. Yarosh
Faculty of Chemistry, Irkutsk State University
Email: aschmidt@chem.isu.ru
Russian Federation, Irkutsk, 664033
N. A. Lagoda
Faculty of Chemistry, Irkutsk State University
Email: aschmidt@chem.isu.ru
Russian Federation, Irkutsk, 664033
A. A. Kurokhtina
Faculty of Chemistry, Irkutsk State University
Email: aschmidt@chem.isu.ru
Russian Federation, Irkutsk, 664033
A. F. Schmidt
Faculty of Chemistry, Irkutsk State University
Author for correspondence.
Email: aschmidt@chem.isu.ru
Russian Federation, Irkutsk, 664033
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