2-Methyl-3-phenylsulfinyl-1-benzofuran

The title compound, C15H12O2S, was prepared by the oxidation of 2-methyl-3-phenylsulfanyl-1-benzofuran with 3-chloroperoxybenzoic acid. The O atom and the phenyl group of the phenylsulfinyl substituent lie on opposite sides of the plane of the benzofuran system. The phenyl ring makes a dihedral angl...

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Main Authors: Hong Dae Choi, Pil Ja Seo, Byeng Wha Son, Uk Lee
Format: Article
Language:English
Published: International Union of Crystallography 2008-08-01
Series:Acta Crystallographica Section E
Online Access:http://scripts.iucr.org/cgi-bin/paper?S1600536808021107
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author Hong Dae Choi
Pil Ja Seo
Byeng Wha Son
Uk Lee
author_facet Hong Dae Choi
Pil Ja Seo
Byeng Wha Son
Uk Lee
author_sort Hong Dae Choi
collection DOAJ
description The title compound, C15H12O2S, was prepared by the oxidation of 2-methyl-3-phenylsulfanyl-1-benzofuran with 3-chloroperoxybenzoic acid. The O atom and the phenyl group of the phenylsulfinyl substituent lie on opposite sides of the plane of the benzofuran system. The phenyl ring makes a dihedral angle of 78.76 (4)° with the benzofuran mean plane. The crystal structure is stabilized by π–π interactions between the furan and benzene rings of neighbouring molecules [centroid–centroid distance = 4.017 (3) Å]. In addition, the crystal structure exhibits intermolecular C—H...π and C—H...O interactions.
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spelling doaj.art-33772b0081d2486db65f50605e4322c12022-12-21T20:05:13ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682008-08-01648o1477o147710.1107/S16005368080211072-Methyl-3-phenylsulfinyl-1-benzofuranHong Dae ChoiPil Ja SeoByeng Wha SonUk LeeThe title compound, C15H12O2S, was prepared by the oxidation of 2-methyl-3-phenylsulfanyl-1-benzofuran with 3-chloroperoxybenzoic acid. The O atom and the phenyl group of the phenylsulfinyl substituent lie on opposite sides of the plane of the benzofuran system. The phenyl ring makes a dihedral angle of 78.76 (4)° with the benzofuran mean plane. The crystal structure is stabilized by π–π interactions between the furan and benzene rings of neighbouring molecules [centroid–centroid distance = 4.017 (3) Å]. In addition, the crystal structure exhibits intermolecular C—H...π and C—H...O interactions.http://scripts.iucr.org/cgi-bin/paper?S1600536808021107
spellingShingle Hong Dae Choi
Pil Ja Seo
Byeng Wha Son
Uk Lee
2-Methyl-3-phenylsulfinyl-1-benzofuran
Acta Crystallographica Section E
title 2-Methyl-3-phenylsulfinyl-1-benzofuran
title_full 2-Methyl-3-phenylsulfinyl-1-benzofuran
title_fullStr 2-Methyl-3-phenylsulfinyl-1-benzofuran
title_full_unstemmed 2-Methyl-3-phenylsulfinyl-1-benzofuran
title_short 2-Methyl-3-phenylsulfinyl-1-benzofuran
title_sort 2 methyl 3 phenylsulfinyl 1 benzofuran
url http://scripts.iucr.org/cgi-bin/paper?S1600536808021107
work_keys_str_mv AT hongdaechoi 2methyl3phenylsulfinyl1benzofuran
AT piljaseo 2methyl3phenylsulfinyl1benzofuran
AT byengwhason 2methyl3phenylsulfinyl1benzofuran
AT uklee 2methyl3phenylsulfinyl1benzofuran