Cargando…

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...

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 2009
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
Descripción
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].