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2-[(5-Chloro-2-oxidobenzylidene)azaniumyl]-2-methylpropane-1,3-diol
The title compound, C(11)H(14)ClNO(3), was prepared by the condensation of equimolar quantities of 5-chlorosalicylaldehyde and 2-amino-2-methylpropane-1,3-diol in methanol. In the crystal, it exists in the zwitterionic form, with nominal proton transfer from the phenol group to the imine N atom....
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3274988/ https://www.ncbi.nlm.nih.gov/pubmed/22346933 http://dx.doi.org/10.1107/S1600536811055784 |
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author | Wang, Dong-Yue Liu, Min Ma, Jing-Jun |
author_facet | Wang, Dong-Yue Liu, Min Ma, Jing-Jun |
author_sort | Wang, Dong-Yue |
collection | PubMed |
description | The title compound, C(11)H(14)ClNO(3), was prepared by the condensation of equimolar quantities of 5-chlorosalicylaldehyde and 2-amino-2-methylpropane-1,3-diol in methanol. In the crystal, it exists in the zwitterionic form, with nominal proton transfer from the phenol group to the imine N atom. This results in the formation of an intramolecular N—H⋯O hydrogen bond, which generates an S(6) ring. Intermolecular O—H⋯O hydrogen bonds arise from the hydroxy groups, forming (001) sheets. |
format | Online Article Text |
id | pubmed-3274988 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-32749882012-02-15 2-[(5-Chloro-2-oxidobenzylidene)azaniumyl]-2-methylpropane-1,3-diol Wang, Dong-Yue Liu, Min Ma, Jing-Jun Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(11)H(14)ClNO(3), was prepared by the condensation of equimolar quantities of 5-chlorosalicylaldehyde and 2-amino-2-methylpropane-1,3-diol in methanol. In the crystal, it exists in the zwitterionic form, with nominal proton transfer from the phenol group to the imine N atom. This results in the formation of an intramolecular N—H⋯O hydrogen bond, which generates an S(6) ring. Intermolecular O—H⋯O hydrogen bonds arise from the hydroxy groups, forming (001) sheets. International Union of Crystallography 2012-01-07 /pmc/articles/PMC3274988/ /pubmed/22346933 http://dx.doi.org/10.1107/S1600536811055784 Text en © Wang et al. 2012 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, Dong-Yue Liu, Min Ma, Jing-Jun 2-[(5-Chloro-2-oxidobenzylidene)azaniumyl]-2-methylpropane-1,3-diol |
title | 2-[(5-Chloro-2-oxidobenzylidene)azaniumyl]-2-methylpropane-1,3-diol |
title_full | 2-[(5-Chloro-2-oxidobenzylidene)azaniumyl]-2-methylpropane-1,3-diol |
title_fullStr | 2-[(5-Chloro-2-oxidobenzylidene)azaniumyl]-2-methylpropane-1,3-diol |
title_full_unstemmed | 2-[(5-Chloro-2-oxidobenzylidene)azaniumyl]-2-methylpropane-1,3-diol |
title_short | 2-[(5-Chloro-2-oxidobenzylidene)azaniumyl]-2-methylpropane-1,3-diol |
title_sort | 2-[(5-chloro-2-oxidobenzylidene)azaniumyl]-2-methylpropane-1,3-diol |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3274988/ https://www.ncbi.nlm.nih.gov/pubmed/22346933 http://dx.doi.org/10.1107/S1600536811055784 |
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