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3-(4-Chlorophenylsulfonyl)-2-methylnaphtho[1,2-b]furan
The title compound, C(19)H(13)ClO(3)S, was prepared by the oxidation of 3-(4-chlorophenylsulfanyl)-2-methylnaphtho[1,2-b]furan with 3-chloroperoxybenzoic acid. The 4-chlorophenyl ring makes a dihedral angle of 68.59 (5)° with the plane of the naphthofuran fragment. The crystal structure is st...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961290/ https://www.ncbi.nlm.nih.gov/pubmed/21202325 http://dx.doi.org/10.1107/S1600536808009215 |
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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(19)H(13)ClO(3)S, was prepared by the oxidation of 3-(4-chlorophenylsulfanyl)-2-methylnaphtho[1,2-b]furan with 3-chloroperoxybenzoic acid. The 4-chlorophenyl ring makes a dihedral angle of 68.59 (5)° with the plane of the naphthofuran fragment. The crystal structure is stabilized by π–π interactions between the benzene rings of neighbouring molecules [centroid–centroid distance = 3.635 (3) Å], and by C—H⋯π interactions between a methyl H atom and the furan ring of an adjacent molecule. In addition, the crystal structure exhibits intermolecular C—H⋯O interactions. |
format | Text |
id | pubmed-2961290 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29612902010-12-30 3-(4-Chlorophenylsulfonyl)-2-methylnaphtho[1,2-b]furan Choi, Hong Dae Seo, Pil Ja Son, Byeng Wha Lee, Uk Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(19)H(13)ClO(3)S, was prepared by the oxidation of 3-(4-chlorophenylsulfanyl)-2-methylnaphtho[1,2-b]furan with 3-chloroperoxybenzoic acid. The 4-chlorophenyl ring makes a dihedral angle of 68.59 (5)° with the plane of the naphthofuran fragment. The crystal structure is stabilized by π–π interactions between the benzene rings of neighbouring molecules [centroid–centroid distance = 3.635 (3) Å], and by C—H⋯π interactions between a methyl H atom and the furan ring of an adjacent molecule. In addition, the crystal structure exhibits intermolecular C—H⋯O interactions. International Union of Crystallography 2008-04-16 /pmc/articles/PMC2961290/ /pubmed/21202325 http://dx.doi.org/10.1107/S1600536808009215 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 3-(4-Chlorophenylsulfonyl)-2-methylnaphtho[1,2-b]furan |
title | 3-(4-Chlorophenylsulfonyl)-2-methylnaphtho[1,2-b]furan |
title_full | 3-(4-Chlorophenylsulfonyl)-2-methylnaphtho[1,2-b]furan |
title_fullStr | 3-(4-Chlorophenylsulfonyl)-2-methylnaphtho[1,2-b]furan |
title_full_unstemmed | 3-(4-Chlorophenylsulfonyl)-2-methylnaphtho[1,2-b]furan |
title_short | 3-(4-Chlorophenylsulfonyl)-2-methylnaphtho[1,2-b]furan |
title_sort | 3-(4-chlorophenylsulfonyl)-2-methylnaphtho[1,2-b]furan |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961290/ https://www.ncbi.nlm.nih.gov/pubmed/21202325 http://dx.doi.org/10.1107/S1600536808009215 |
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