(E)-Methyl 3-(3,4-dihy­droxy­phen­yl)acrylate

The benzene ring in the title compound, C(10)H(10)O(4), makes an angle of 4.4 (1)° with the C—C—C—O linker. The hy­droxy groups are involved in both intra- and inter­molecular O—H⋯O hydrogen bonds. The crystal packing is stabilized by O—H⋯O hydrogen-bonding inter­actions. The mol­ecules of the caffe...

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Detalles Bibliográficos
Autores principales: Wang, Li, Meng, Fa-Yan, Lin, Cui-Wu, Chen, Hai-Yan, Luo, Xuan
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051619/
https://www.ncbi.nlm.nih.gov/pubmed/21523034
http://dx.doi.org/10.1107/S1600536810054504
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author Wang, Li
Meng, Fa-Yan
Lin, Cui-Wu
Chen, Hai-Yan
Luo, Xuan
author_facet Wang, Li
Meng, Fa-Yan
Lin, Cui-Wu
Chen, Hai-Yan
Luo, Xuan
author_sort Wang, Li
collection PubMed
description The benzene ring in the title compound, C(10)H(10)O(4), makes an angle of 4.4 (1)° with the C—C—C—O linker. The hy­droxy groups are involved in both intra- and inter­molecular O—H⋯O hydrogen bonds. The crystal packing is stabilized by O—H⋯O hydrogen-bonding inter­actions. The mol­ecules of the caffeic acid ester form a dimeric structure in a head-to-head manner along the a axis through O—H⋯O hydrogen bonds. The dimers inter­act with one another through O—H⋯O hydrogen bonds, forming supermolecular chains. These chains are further extended through C—H⋯O hydrogen bonds as well as van der Waals inter­actions into the final three-dimensional architecture.
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spelling pubmed-30516192011-04-26 (E)-Methyl 3-(3,4-dihy­droxy­phen­yl)acrylate Wang, Li Meng, Fa-Yan Lin, Cui-Wu Chen, Hai-Yan Luo, Xuan Acta Crystallogr Sect E Struct Rep Online Organic Papers The benzene ring in the title compound, C(10)H(10)O(4), makes an angle of 4.4 (1)° with the C—C—C—O linker. The hy­droxy groups are involved in both intra- and inter­molecular O—H⋯O hydrogen bonds. The crystal packing is stabilized by O—H⋯O hydrogen-bonding inter­actions. The mol­ecules of the caffeic acid ester form a dimeric structure in a head-to-head manner along the a axis through O—H⋯O hydrogen bonds. The dimers inter­act with one another through O—H⋯O hydrogen bonds, forming supermolecular chains. These chains are further extended through C—H⋯O hydrogen bonds as well as van der Waals inter­actions into the final three-dimensional architecture. International Union of Crystallography 2011-01-12 /pmc/articles/PMC3051619/ /pubmed/21523034 http://dx.doi.org/10.1107/S1600536810054504 Text en © Wang 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
Wang, Li
Meng, Fa-Yan
Lin, Cui-Wu
Chen, Hai-Yan
Luo, Xuan
(E)-Methyl 3-(3,4-dihy­droxy­phen­yl)acrylate
title (E)-Methyl 3-(3,4-dihy­droxy­phen­yl)acrylate
title_full (E)-Methyl 3-(3,4-dihy­droxy­phen­yl)acrylate
title_fullStr (E)-Methyl 3-(3,4-dihy­droxy­phen­yl)acrylate
title_full_unstemmed (E)-Methyl 3-(3,4-dihy­droxy­phen­yl)acrylate
title_short (E)-Methyl 3-(3,4-dihy­droxy­phen­yl)acrylate
title_sort (e)-methyl 3-(3,4-dihy­droxy­phen­yl)acrylate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051619/
https://www.ncbi.nlm.nih.gov/pubmed/21523034
http://dx.doi.org/10.1107/S1600536810054504
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