5-Bromo-3-cyclo­hexyl­sulfonyl-2-methyl-1-benzofuran

In the title compound, C(15)H(17)BrO(3)S, the cyclo­hexyl ring adopts a practically undistorted chair conformation [endocyclic torsion angles are within a 54.5–56.4 (3)° range] and the aryl­sulfonyl unit is positioned equatorial relative to the cyclo­hexyl group. In the crystal, mol­ecules are linke...

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Detalles Bibliográficos
Autores principales: Choi, Hong Dae, Seo, Pil Ja, Son, Byeng Wha, Lee, Uk
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3052108/
https://www.ncbi.nlm.nih.gov/pubmed/21522310
http://dx.doi.org/10.1107/S1600536811003515
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author Choi, Hong Dae
Seo, Pil Ja
Son, Byeng Wha
Lee, Uk
author_facet Choi, Hong Dae
Seo, Pil Ja
Son, Byeng Wha
Lee, Uk
author_sort Choi, Hong Dae
collection PubMed
description In the title compound, C(15)H(17)BrO(3)S, the cyclo­hexyl ring adopts a practically undistorted chair conformation [endocyclic torsion angles are within a 54.5–56.4 (3)° range] and the aryl­sulfonyl unit is positioned equatorial relative to the cyclo­hexyl group. In the crystal, mol­ecules are linked through C—H⋯O hydrogen bonds and donor–acceptor Br⋯O contacts [3.250 (2) Å]. The crystal structure also exhibits aromatic π–π overlap between the benzene and furan rings of neighbouring mol­ecules [centroid–centroid distance = 3.635 (2) Å].
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spelling pubmed-30521082011-04-26 5-Bromo-3-cyclo­hexyl­sulfonyl-2-methyl-1-benzofuran Choi, Hong Dae Seo, Pil Ja Son, Byeng Wha Lee, Uk Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(15)H(17)BrO(3)S, the cyclo­hexyl ring adopts a practically undistorted chair conformation [endocyclic torsion angles are within a 54.5–56.4 (3)° range] and the aryl­sulfonyl unit is positioned equatorial relative to the cyclo­hexyl group. In the crystal, mol­ecules are linked through C—H⋯O hydrogen bonds and donor–acceptor Br⋯O contacts [3.250 (2) Å]. The crystal structure also exhibits aromatic π–π overlap between the benzene and furan rings of neighbouring mol­ecules [centroid–centroid distance = 3.635 (2) Å]. International Union of Crystallography 2011-02-02 /pmc/articles/PMC3052108/ /pubmed/21522310 http://dx.doi.org/10.1107/S1600536811003515 Text en © Choi 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
Choi, Hong Dae
Seo, Pil Ja
Son, Byeng Wha
Lee, Uk
5-Bromo-3-cyclo­hexyl­sulfonyl-2-methyl-1-benzofuran
title 5-Bromo-3-cyclo­hexyl­sulfonyl-2-methyl-1-benzofuran
title_full 5-Bromo-3-cyclo­hexyl­sulfonyl-2-methyl-1-benzofuran
title_fullStr 5-Bromo-3-cyclo­hexyl­sulfonyl-2-methyl-1-benzofuran
title_full_unstemmed 5-Bromo-3-cyclo­hexyl­sulfonyl-2-methyl-1-benzofuran
title_short 5-Bromo-3-cyclo­hexyl­sulfonyl-2-methyl-1-benzofuran
title_sort 5-bromo-3-cyclo­hexyl­sulfonyl-2-methyl-1-benzofuran
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3052108/
https://www.ncbi.nlm.nih.gov/pubmed/21522310
http://dx.doi.org/10.1107/S1600536811003515
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AT sonbyengwha 5bromo3cyclohexylsulfonyl2methyl1benzofuran
AT leeuk 5bromo3cyclohexylsulfonyl2methyl1benzofuran

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