Cargando…
Methyl 2-(5-bromo-3-methylsulfinyl-1-benzofuran-2-yl)acetate
The title compound, C(12)H(11)BrO(4)S, was synthesized by the oxidation of methyl 2-(5-bromo-3-methylsulfanyl-1-benzofuran-2-yl)acetate with 3-chloroperoxybenzoic acid. The O atom and the methyl group of the methylsulfinyl substituent lie on opposite sides of the plane of the benzofuran ring sys...
Autores principales: | , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2008
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959898/ https://www.ncbi.nlm.nih.gov/pubmed/21581367 http://dx.doi.org/10.1107/S1600536808037768 |
_version_ | 1782188609997111296 |
---|---|
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(12)H(11)BrO(4)S, was synthesized by the oxidation of methyl 2-(5-bromo-3-methylsulfanyl-1-benzofuran-2-yl)acetate with 3-chloroperoxybenzoic acid. The O atom and the methyl group of the methylsulfinyl substituent lie on opposite sides of the plane of the benzofuran ring system. The crystal structure is stabilized by C—H⋯π interactions, involving a methyl H atom and the benzene ring of a neighbouring molecule, and by weak intermolecular C—H⋯O hydrogen bonds. |
format | Text |
id | pubmed-2959898 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29598982010-12-30 Methyl 2-(5-bromo-3-methylsulfinyl-1-benzofuran-2-yl)acetate Choi, Hong Dae Seo, Pil Ja Son, Byeng Wha Lee, Uk Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(12)H(11)BrO(4)S, was synthesized by the oxidation of methyl 2-(5-bromo-3-methylsulfanyl-1-benzofuran-2-yl)acetate with 3-chloroperoxybenzoic acid. The O atom and the methyl group of the methylsulfinyl substituent lie on opposite sides of the plane of the benzofuran ring system. The crystal structure is stabilized by C—H⋯π interactions, involving a methyl H atom and the benzene ring of a neighbouring molecule, and by weak intermolecular C—H⋯O hydrogen bonds. International Union of Crystallography 2008-11-20 /pmc/articles/PMC2959898/ /pubmed/21581367 http://dx.doi.org/10.1107/S1600536808037768 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 Methyl 2-(5-bromo-3-methylsulfinyl-1-benzofuran-2-yl)acetate |
title | Methyl 2-(5-bromo-3-methylsulfinyl-1-benzofuran-2-yl)acetate |
title_full | Methyl 2-(5-bromo-3-methylsulfinyl-1-benzofuran-2-yl)acetate |
title_fullStr | Methyl 2-(5-bromo-3-methylsulfinyl-1-benzofuran-2-yl)acetate |
title_full_unstemmed | Methyl 2-(5-bromo-3-methylsulfinyl-1-benzofuran-2-yl)acetate |
title_short | Methyl 2-(5-bromo-3-methylsulfinyl-1-benzofuran-2-yl)acetate |
title_sort | methyl 2-(5-bromo-3-methylsulfinyl-1-benzofuran-2-yl)acetate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959898/ https://www.ncbi.nlm.nih.gov/pubmed/21581367 http://dx.doi.org/10.1107/S1600536808037768 |
work_keys_str_mv | AT choihongdae methyl25bromo3methylsulfinyl1benzofuran2ylacetate AT seopilja methyl25bromo3methylsulfinyl1benzofuran2ylacetate AT sonbyengwha methyl25bromo3methylsulfinyl1benzofuran2ylacetate AT leeuk methyl25bromo3methylsulfinyl1benzofuran2ylacetate |