3-(4-Bromo­phen­yl)-4-(4-hy­droxy­anilino)furan-2(5H)-one

In the title compound, C(16)H(12)BrNO(3), the butyrolactone core adopts the furan-2(5H)-one structure and forms dihedral angles of 44.80 (17) and 65.73 (18)° with the bromo­benzene and phenol rings, respectively. In the crystal, N—H⋯O and O—H⋯O hydrogen bonds link the mol­ecules, generating R (4) (3...

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Detalles Bibliográficos
Autores principales: Peng, Wanxi, Wang, Lansheng, Wu, Fengjuan, Xu, Qiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3200956/
https://www.ncbi.nlm.nih.gov/pubmed/22058954
http://dx.doi.org/10.1107/S1600536811031849
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author Peng, Wanxi
Wang, Lansheng
Wu, Fengjuan
Xu, Qiu
author_facet Peng, Wanxi
Wang, Lansheng
Wu, Fengjuan
Xu, Qiu
author_sort Peng, Wanxi
collection PubMed
description In the title compound, C(16)H(12)BrNO(3), the butyrolactone core adopts the furan-2(5H)-one structure and forms dihedral angles of 44.80 (17) and 65.73 (18)° with the bromo­benzene and phenol rings, respectively. In the crystal, N—H⋯O and O—H⋯O hydrogen bonds link the mol­ecules, generating R (4) (3)(26) loops The edge-fused rings extend to form a chain running along the b-axis direction and C—H⋯π contacts help to consolidate the packing.
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spelling pubmed-32009562011-11-06 3-(4-Bromo­phen­yl)-4-(4-hy­droxy­anilino)furan-2(5H)-one Peng, Wanxi Wang, Lansheng Wu, Fengjuan Xu, Qiu Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(16)H(12)BrNO(3), the butyrolactone core adopts the furan-2(5H)-one structure and forms dihedral angles of 44.80 (17) and 65.73 (18)° with the bromo­benzene and phenol rings, respectively. In the crystal, N—H⋯O and O—H⋯O hydrogen bonds link the mol­ecules, generating R (4) (3)(26) loops The edge-fused rings extend to form a chain running along the b-axis direction and C—H⋯π contacts help to consolidate the packing. International Union of Crystallography 2011-08-11 /pmc/articles/PMC3200956/ /pubmed/22058954 http://dx.doi.org/10.1107/S1600536811031849 Text en © Peng et al. 2011 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
Peng, Wanxi
Wang, Lansheng
Wu, Fengjuan
Xu, Qiu
3-(4-Bromo­phen­yl)-4-(4-hy­droxy­anilino)furan-2(5H)-one
title 3-(4-Bromo­phen­yl)-4-(4-hy­droxy­anilino)furan-2(5H)-one
title_full 3-(4-Bromo­phen­yl)-4-(4-hy­droxy­anilino)furan-2(5H)-one
title_fullStr 3-(4-Bromo­phen­yl)-4-(4-hy­droxy­anilino)furan-2(5H)-one
title_full_unstemmed 3-(4-Bromo­phen­yl)-4-(4-hy­droxy­anilino)furan-2(5H)-one
title_short 3-(4-Bromo­phen­yl)-4-(4-hy­droxy­anilino)furan-2(5H)-one
title_sort 3-(4-bromo­phen­yl)-4-(4-hy­droxy­anilino)furan-2(5h)-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3200956/
https://www.ncbi.nlm.nih.gov/pubmed/22058954
http://dx.doi.org/10.1107/S1600536811031849
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AT xuqiu 34bromophenyl44hydroxyanilinofuran25hone

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