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6-Methyl-2,4-diphenyl­quinoline

The mol­ecules of the title compound, C(22)H(17)N, are linked by weak inter­actions, among which the most prominent are C—H⋯π inter­actions. The dihedral angles between the phenyl rings and the quinoline ring system are 43.3 (3) and 21.4 (3)°. The title product resulted from a three-component reacti...

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Detalles Bibliográficos
Autores principales: Huo, Xing, Xu, Yanfen, Li, Xinyun, Pan, Xinfu
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961894/
https://www.ncbi.nlm.nih.gov/pubmed/21202829
http://dx.doi.org/10.1107/S1600536808015651
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author Huo, Xing
Xu, Yanfen
Li, Xinyun
Pan, Xinfu
author_facet Huo, Xing
Xu, Yanfen
Li, Xinyun
Pan, Xinfu
author_sort Huo, Xing
collection PubMed
description The mol­ecules of the title compound, C(22)H(17)N, are linked by weak inter­actions, among which the most prominent are C—H⋯π inter­actions. The dihedral angles between the phenyl rings and the quinoline ring system are 43.3 (3) and 21.4 (3)°. The title product resulted from a three-component reaction of benzaldehyde, 1-ethynylbenzene and p-toluidine via C—H activation of 1-ethynylbenzene catalyzed by CuI in the ionic liquid 1-butyl-3-methyl­imidazolium hexa­fluoro­phosphate.
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spelling pubmed-29618942010-12-30 6-Methyl-2,4-diphenyl­quinoline Huo, Xing Xu, Yanfen Li, Xinyun Pan, Xinfu Acta Crystallogr Sect E Struct Rep Online Organic Papers The mol­ecules of the title compound, C(22)H(17)N, are linked by weak inter­actions, among which the most prominent are C—H⋯π inter­actions. The dihedral angles between the phenyl rings and the quinoline ring system are 43.3 (3) and 21.4 (3)°. The title product resulted from a three-component reaction of benzaldehyde, 1-ethynylbenzene and p-toluidine via C—H activation of 1-ethynylbenzene catalyzed by CuI in the ionic liquid 1-butyl-3-methyl­imidazolium hexa­fluoro­phosphate. International Union of Crystallography 2008-06-07 /pmc/articles/PMC2961894/ /pubmed/21202829 http://dx.doi.org/10.1107/S1600536808015651 Text en © Huo et al. 2008 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Organic Papers
Huo, Xing
Xu, Yanfen
Li, Xinyun
Pan, Xinfu
6-Methyl-2,4-diphenyl­quinoline
title 6-Methyl-2,4-diphenyl­quinoline
title_full 6-Methyl-2,4-diphenyl­quinoline
title_fullStr 6-Methyl-2,4-diphenyl­quinoline
title_full_unstemmed 6-Methyl-2,4-diphenyl­quinoline
title_short 6-Methyl-2,4-diphenyl­quinoline
title_sort 6-methyl-2,4-diphenyl­quinoline
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961894/
https://www.ncbi.nlm.nih.gov/pubmed/21202829
http://dx.doi.org/10.1107/S1600536808015651
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