(E)-2-[(2-Hydroxy­ethyl)iminiometh­yl]-6-methoxy­phenolate

The title Schiff base compound, C(10)H(13)NO(3), obtained by the reaction of 2-hydr­oxy-3-methoxy­benzaldehyde and 2-amino­ethanol in methanol solution, crystallizes in a zwitterionic form, in which the mol­ecule adopts a trans configuration about the central C=N bond. An intra­molecular N—H⋯O hydro...

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Detalles Bibliográficos
Autores principales: Tan, Guo-Xia, Liu, Xi-Cheng
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968608/
https://www.ncbi.nlm.nih.gov/pubmed/21582217
http://dx.doi.org/10.1107/S1600536809005297
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author Tan, Guo-Xia
Liu, Xi-Cheng
author_facet Tan, Guo-Xia
Liu, Xi-Cheng
author_sort Tan, Guo-Xia
collection PubMed
description The title Schiff base compound, C(10)H(13)NO(3), obtained by the reaction of 2-hydr­oxy-3-methoxy­benzaldehyde and 2-amino­ethanol in methanol solution, crystallizes in a zwitterionic form, in which the mol­ecule adopts a trans configuration about the central C=N bond. An intra­molecular N—H⋯O hydrogen bond occurs. In the crystal structure, mol­ecules are linked into chains by inter­molecular O—H⋯O hydrogen bonding.
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spelling pubmed-29686082010-12-30 (E)-2-[(2-Hydroxy­ethyl)iminiometh­yl]-6-methoxy­phenolate Tan, Guo-Xia Liu, Xi-Cheng Acta Crystallogr Sect E Struct Rep Online Organic Papers The title Schiff base compound, C(10)H(13)NO(3), obtained by the reaction of 2-hydr­oxy-3-methoxy­benzaldehyde and 2-amino­ethanol in methanol solution, crystallizes in a zwitterionic form, in which the mol­ecule adopts a trans configuration about the central C=N bond. An intra­molecular N—H⋯O hydrogen bond occurs. In the crystal structure, mol­ecules are linked into chains by inter­molecular O—H⋯O hydrogen bonding. International Union of Crystallography 2009-02-21 /pmc/articles/PMC2968608/ /pubmed/21582217 http://dx.doi.org/10.1107/S1600536809005297 Text en © Tan and Liu 2009 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
Tan, Guo-Xia
Liu, Xi-Cheng
(E)-2-[(2-Hydroxy­ethyl)iminiometh­yl]-6-methoxy­phenolate
title (E)-2-[(2-Hydroxy­ethyl)iminiometh­yl]-6-methoxy­phenolate
title_full (E)-2-[(2-Hydroxy­ethyl)iminiometh­yl]-6-methoxy­phenolate
title_fullStr (E)-2-[(2-Hydroxy­ethyl)iminiometh­yl]-6-methoxy­phenolate
title_full_unstemmed (E)-2-[(2-Hydroxy­ethyl)iminiometh­yl]-6-methoxy­phenolate
title_short (E)-2-[(2-Hydroxy­ethyl)iminiometh­yl]-6-methoxy­phenolate
title_sort (e)-2-[(2-hydroxy­ethyl)iminiometh­yl]-6-methoxy­phenolate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968608/
https://www.ncbi.nlm.nih.gov/pubmed/21582217
http://dx.doi.org/10.1107/S1600536809005297
work_keys_str_mv AT tanguoxia e22hydroxyethyliminiomethyl6methoxyphenolate
AT liuxicheng e22hydroxyethyliminiomethyl6methoxyphenolate

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