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4-tert-Butyl-3′,4′-bis­(4-methyl­phen­yl)-3,4-dihydro-1H,4′H-spiro­[naphthalene-2,5′-[1,2]oxazol]-1-one

In the title compound, C(30)H(31)NO(2), the cyclo­hexa­none ring in the naphthalene fused-ring system adopts a half-chair conformation, presumably due to conjugation of the benzene ring. The naphthalene ring system makes dihedral angles of 86.63 (7), 65.15 (8) and 63.18 (8)° with respect to the two...

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Autores principales: Akhazzane, Mohamed, Zouihri, Hafid, Bennani, A.Kella, Kerbal, Abdelali, Al Houari, Ghali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3152001/
https://www.ncbi.nlm.nih.gov/pubmed/21837226
http://dx.doi.org/10.1107/S1600536811025086
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author Akhazzane, Mohamed
Zouihri, Hafid
Bennani, A.Kella
Kerbal, Abdelali
Al Houari, Ghali
author_facet Akhazzane, Mohamed
Zouihri, Hafid
Bennani, A.Kella
Kerbal, Abdelali
Al Houari, Ghali
author_sort Akhazzane, Mohamed
collection PubMed
description In the title compound, C(30)H(31)NO(2), the cyclo­hexa­none ring in the naphthalene fused-ring system adopts a half-chair conformation, presumably due to conjugation of the benzene ring. The naphthalene ring system makes dihedral angles of 86.63 (7), 65.15 (8) and 63.18 (8)° with respect to the two methyl­benzene planes and the 1,2-oxazole ring system. Inter­molecular C—H⋯O and C—H⋯N hydrogen bonding and C—H⋯π inter­actions stabilize the crystal structure. The H atoms of the two methyl groups of the methyl­phenyl groups are disordered over two positions with equal occupancies.
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spelling pubmed-31520012011-08-11 4-tert-Butyl-3′,4′-bis­(4-methyl­phen­yl)-3,4-dihydro-1H,4′H-spiro­[naphthalene-2,5′-[1,2]oxazol]-1-one Akhazzane, Mohamed Zouihri, Hafid Bennani, A.Kella Kerbal, Abdelali Al Houari, Ghali Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(30)H(31)NO(2), the cyclo­hexa­none ring in the naphthalene fused-ring system adopts a half-chair conformation, presumably due to conjugation of the benzene ring. The naphthalene ring system makes dihedral angles of 86.63 (7), 65.15 (8) and 63.18 (8)° with respect to the two methyl­benzene planes and the 1,2-oxazole ring system. Inter­molecular C—H⋯O and C—H⋯N hydrogen bonding and C—H⋯π inter­actions stabilize the crystal structure. The H atoms of the two methyl groups of the methyl­phenyl groups are disordered over two positions with equal occupancies. International Union of Crystallography 2011-06-30 /pmc/articles/PMC3152001/ /pubmed/21837226 http://dx.doi.org/10.1107/S1600536811025086 Text en © Akhazzane et al. 2011 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
Akhazzane, Mohamed
Zouihri, Hafid
Bennani, A.Kella
Kerbal, Abdelali
Al Houari, Ghali
4-tert-Butyl-3′,4′-bis­(4-methyl­phen­yl)-3,4-dihydro-1H,4′H-spiro­[naphthalene-2,5′-[1,2]oxazol]-1-one
title 4-tert-Butyl-3′,4′-bis­(4-methyl­phen­yl)-3,4-dihydro-1H,4′H-spiro­[naphthalene-2,5′-[1,2]oxazol]-1-one
title_full 4-tert-Butyl-3′,4′-bis­(4-methyl­phen­yl)-3,4-dihydro-1H,4′H-spiro­[naphthalene-2,5′-[1,2]oxazol]-1-one
title_fullStr 4-tert-Butyl-3′,4′-bis­(4-methyl­phen­yl)-3,4-dihydro-1H,4′H-spiro­[naphthalene-2,5′-[1,2]oxazol]-1-one
title_full_unstemmed 4-tert-Butyl-3′,4′-bis­(4-methyl­phen­yl)-3,4-dihydro-1H,4′H-spiro­[naphthalene-2,5′-[1,2]oxazol]-1-one
title_short 4-tert-Butyl-3′,4′-bis­(4-methyl­phen­yl)-3,4-dihydro-1H,4′H-spiro­[naphthalene-2,5′-[1,2]oxazol]-1-one
title_sort 4-tert-butyl-3′,4′-bis­(4-methyl­phen­yl)-3,4-dihydro-1h,4′h-spiro­[naphthalene-2,5′-[1,2]oxazol]-1-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3152001/
https://www.ncbi.nlm.nih.gov/pubmed/21837226
http://dx.doi.org/10.1107/S1600536811025086
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