Isopropyl 2-(5-methyl-3-methyl­sulfinyl-1-benzofuran-2-yl)acetate

The title compound, C(15)H(18)O(4)S, was prepared by the oxidation of isopropyl 2-(5-methyl-3-methyl­sulfanyl-1-benzofuran-2-yl)acetate with 3-chloro­peroxy­benzoic acid. The crystal structure is stabilized by inter­molecular π–π inter­actions between the benzene rings; the centroid–centroid distanc...

Descripción completa

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/PMC2959682/
https://www.ncbi.nlm.nih.gov/pubmed/21580944
http://dx.doi.org/10.1107/S1600536808031796
_version_ 1782188558156562432
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(15)H(18)O(4)S, was prepared by the oxidation of isopropyl 2-(5-methyl-3-methyl­sulfanyl-1-benzofuran-2-yl)acetate with 3-chloro­peroxy­benzoic acid. The crystal structure is stabilized by inter­molecular π–π inter­actions between the benzene rings; the centroid–centroid distance between the adjacent benzene rings (symmetry code: [Image: see text]) is 3.713 (2) Å. In addition, C—H⋯π and weak inter­molecular C—H⋯O inter­actions are present in the structure.
format Text
id pubmed-2959682
institution National Center for Biotechnology Information
language English
publishDate 2008
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-29596822010-12-30 Isopropyl 2-(5-methyl-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(15)H(18)O(4)S, was prepared by the oxidation of isopropyl 2-(5-methyl-3-methyl­sulfanyl-1-benzofuran-2-yl)acetate with 3-chloro­peroxy­benzoic acid. The crystal structure is stabilized by inter­molecular π–π inter­actions between the benzene rings; the centroid–centroid distance between the adjacent benzene rings (symmetry code: [Image: see text]) is 3.713 (2) Å. In addition, C—H⋯π and weak inter­molecular C—H⋯O inter­actions are present in the structure. International Union of Crystallography 2008-10-09 /pmc/articles/PMC2959682/ /pubmed/21580944 http://dx.doi.org/10.1107/S1600536808031796 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
Isopropyl 2-(5-methyl-3-methyl­sulfinyl-1-benzofuran-2-yl)acetate
title Isopropyl 2-(5-methyl-3-methyl­sulfinyl-1-benzofuran-2-yl)acetate
title_full Isopropyl 2-(5-methyl-3-methyl­sulfinyl-1-benzofuran-2-yl)acetate
title_fullStr Isopropyl 2-(5-methyl-3-methyl­sulfinyl-1-benzofuran-2-yl)acetate
title_full_unstemmed Isopropyl 2-(5-methyl-3-methyl­sulfinyl-1-benzofuran-2-yl)acetate
title_short Isopropyl 2-(5-methyl-3-methyl­sulfinyl-1-benzofuran-2-yl)acetate
title_sort isopropyl 2-(5-methyl-3-methyl­sulfinyl-1-benzofuran-2-yl)acetate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959682/
https://www.ncbi.nlm.nih.gov/pubmed/21580944
http://dx.doi.org/10.1107/S1600536808031796
work_keys_str_mv AT choihongdae isopropyl25methyl3methylsulfinyl1benzofuran2ylacetate
AT seopilja isopropyl25methyl3methylsulfinyl1benzofuran2ylacetate
AT sonbyengwha isopropyl25methyl3methylsulfinyl1benzofuran2ylacetate
AT leeuk isopropyl25methyl3methylsulfinyl1benzofuran2ylacetate

Ejemplares similares