2,5-Dimethyl-3-phenyl­sulfonyl-1-benzofuran

The title compound, C(16)H(14)O(3)S, was prepared by the oxidation of 2,5-dimethyl-3-phenyl­sulfanyl-1-benzofuran with 3-chloro­peroxy­benzoic acid. The phenyl ring makes a dihedral angle of 76.98 (9)° with the plane of the benzofuran fragment. The crystal structure is stabilized by π–π inter­action...

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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 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961094/
https://www.ncbi.nlm.nih.gov/pubmed/21202338
http://dx.doi.org/10.1107/S1600536808009811
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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 The title compound, C(16)H(14)O(3)S, was prepared by the oxidation of 2,5-dimethyl-3-phenyl­sulfanyl-1-benzofuran with 3-chloro­peroxy­benzoic acid. The phenyl ring makes a dihedral angle of 76.98 (9)° with the plane of the benzofuran fragment. The crystal structure is stabilized by π–π inter­actions between furan and benzene rings of neighbouring mol­ecules [centroid–centroid distance = 3.775 (4) Å]. In addition, the crystal structure exhibits intra- and inter­molecular C—H⋯O inter­actions.
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spelling pubmed-29610942010-12-30 2,5-Dimethyl-3-phenyl­sulfonyl-1-benzofuran Choi, Hong Dae Seo, Pil Ja Son, Byeng Wha Lee, Uk Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(16)H(14)O(3)S, was prepared by the oxidation of 2,5-dimethyl-3-phenyl­sulfanyl-1-benzofuran with 3-chloro­peroxy­benzoic acid. The phenyl ring makes a dihedral angle of 76.98 (9)° with the plane of the benzofuran fragment. The crystal structure is stabilized by π–π inter­actions between furan and benzene rings of neighbouring mol­ecules [centroid–centroid distance = 3.775 (4) Å]. In addition, the crystal structure exhibits intra- and inter­molecular C—H⋯O inter­actions. International Union of Crystallography 2008-04-16 /pmc/articles/PMC2961094/ /pubmed/21202338 http://dx.doi.org/10.1107/S1600536808009811 Text en © Choi 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
Choi, Hong Dae
Seo, Pil Ja
Son, Byeng Wha
Lee, Uk
2,5-Dimethyl-3-phenyl­sulfonyl-1-benzofuran
title 2,5-Dimethyl-3-phenyl­sulfonyl-1-benzofuran
title_full 2,5-Dimethyl-3-phenyl­sulfonyl-1-benzofuran
title_fullStr 2,5-Dimethyl-3-phenyl­sulfonyl-1-benzofuran
title_full_unstemmed 2,5-Dimethyl-3-phenyl­sulfonyl-1-benzofuran
title_short 2,5-Dimethyl-3-phenyl­sulfonyl-1-benzofuran
title_sort 2,5-dimethyl-3-phenyl­sulfonyl-1-benzofuran
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961094/
https://www.ncbi.nlm.nih.gov/pubmed/21202338
http://dx.doi.org/10.1107/S1600536808009811
work_keys_str_mv AT choihongdae 25dimethyl3phenylsulfonyl1benzofuran
AT seopilja 25dimethyl3phenylsulfonyl1benzofuran
AT sonbyengwha 25dimethyl3phenylsulfonyl1benzofuran
AT leeuk 25dimethyl3phenylsulfonyl1benzofuran

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