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2-(3-Ethylsulfanyl-5-fluoro-1-benzofuran-2-yl)acetic acid
The title compound, C(12)H(11)FO(3)S, was prepared by alkaline hydrolysis of ethyl 2–(3–ethylsulfanyl–5–fluoro–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. The...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2970325/ https://www.ncbi.nlm.nih.gov/pubmed/21577933 http://dx.doi.org/10.1107/S160053680903671X |
Sumario: | The title compound, C(12)H(11)FO(3)S, was prepared by alkaline hydrolysis of ethyl 2–(3–ethylsulfanyl–5–fluoro–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 aromatic π–π interactions between the furan ring and the benzene ring of neighbouring benzofuran ring systems [centroid–centroid distance = 3.684 (5) Å]. |
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