2-(5-Fluoro-3-methyl­sulfanyl-1-benzofuran-2-yl)acetic acid

The title compound, C(11)H(9)FO(3)S, was prepared by alkaline hydrolysis of ethyl 2-(5-fluoro-3-methyl­sulfanyl-1-benzofuran-2-yl)acetate. In the crystal structure, the carboxyl groups are involved in inter­molecular O—H⋯O hydrogen bonds, which link the mol­ecules into centrosymmetric dimers. These...

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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 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977173/
https://www.ncbi.nlm.nih.gov/pubmed/21583516
http://dx.doi.org/10.1107/S160053680902594X
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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(11)H(9)FO(3)S, was prepared by alkaline hydrolysis of ethyl 2-(5-fluoro-3-methyl­sulfanyl-1-benzofuran-2-yl)acetate. In the crystal structure, the carboxyl groups are involved in inter­molecular O—H⋯O hydrogen bonds, which link the mol­ecules into centrosymmetric dimers. These dimers are further packed into stacks along the b axis by inter­molecular C—H⋯O and C—H⋯F inter­actions.
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spelling pubmed-29771732010-12-30 2-(5-Fluoro-3-methyl­sulfanyl-1-benzofuran-2-yl)acetic acid Choi, Hong Dae Seo, Pil Ja Son, Byeng Wha Lee, Uk Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(11)H(9)FO(3)S, was prepared by alkaline hydrolysis of ethyl 2-(5-fluoro-3-methyl­sulfanyl-1-benzofuran-2-yl)acetate. In the crystal structure, the carboxyl groups are involved in inter­molecular O—H⋯O hydrogen bonds, which link the mol­ecules into centrosymmetric dimers. These dimers are further packed into stacks along the b axis by inter­molecular C—H⋯O and C—H⋯F inter­actions. International Union of Crystallography 2009-07-11 /pmc/articles/PMC2977173/ /pubmed/21583516 http://dx.doi.org/10.1107/S160053680902594X Text en © Choi et al. 2009 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-Fluoro-3-methyl­sulfanyl-1-benzofuran-2-yl)acetic acid
title 2-(5-Fluoro-3-methyl­sulfanyl-1-benzofuran-2-yl)acetic acid
title_full 2-(5-Fluoro-3-methyl­sulfanyl-1-benzofuran-2-yl)acetic acid
title_fullStr 2-(5-Fluoro-3-methyl­sulfanyl-1-benzofuran-2-yl)acetic acid
title_full_unstemmed 2-(5-Fluoro-3-methyl­sulfanyl-1-benzofuran-2-yl)acetic acid
title_short 2-(5-Fluoro-3-methyl­sulfanyl-1-benzofuran-2-yl)acetic acid
title_sort 2-(5-fluoro-3-methyl­sulfanyl-1-benzofuran-2-yl)acetic acid
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977173/
https://www.ncbi.nlm.nih.gov/pubmed/21583516
http://dx.doi.org/10.1107/S160053680902594X
work_keys_str_mv AT choihongdae 25fluoro3methylsulfanyl1benzofuran2ylaceticacid
AT seopilja 25fluoro3methylsulfanyl1benzofuran2ylaceticacid
AT sonbyengwha 25fluoro3methylsulfanyl1benzofuran2ylaceticacid
AT leeuk 25fluoro3methylsulfanyl1benzofuran2ylaceticacid

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