4-(2-Hy­droxy­eth­oxy)phenol

The asymmetric unit of the title compound, C(8)H(10)O(3), contains four mol­ecules, which differ in the orientation of the hy­­droxy­ethyl group [O—C—C—O torsion angles = −168.89 (17), 72.9 (2), −65.8 (2) and 71.8 (2)°], as well as the orientation of the hy­droxy H atoms. Furthermore, the crystal st...

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Detalles Bibliográficos
Autores principales: Meister, Anne C., Lang, Mathias, Nieger, Martin, Bräse, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3793793/
https://www.ncbi.nlm.nih.gov/pubmed/24109380
http://dx.doi.org/10.1107/S1600536813019818
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author Meister, Anne C.
Lang, Mathias
Nieger, Martin
Bräse, Stefan
author_facet Meister, Anne C.
Lang, Mathias
Nieger, Martin
Bräse, Stefan
author_sort Meister, Anne C.
collection PubMed
description The asymmetric unit of the title compound, C(8)H(10)O(3), contains four mol­ecules, which differ in the orientation of the hy­­droxy­ethyl group [O—C—C—O torsion angles = −168.89 (17), 72.9 (2), −65.8 (2) and 71.8 (2)°], as well as the orientation of the hy­droxy H atoms. Furthermore, the crystal structure displays two different types of strong hydrogen bond. The first is between an alcohol O—H and another alcohol O atom, and the second between an alcohol O—H group and an ether O atom. Additional weak hydrogen bonds between C—H groups and ether O atoms stabilize the structure.
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spelling pubmed-37937932013-10-09 4-(2-Hy­droxy­eth­oxy)phenol Meister, Anne C. Lang, Mathias Nieger, Martin Bräse, Stefan Acta Crystallogr Sect E Struct Rep Online Organic Papers The asymmetric unit of the title compound, C(8)H(10)O(3), contains four mol­ecules, which differ in the orientation of the hy­­droxy­ethyl group [O—C—C—O torsion angles = −168.89 (17), 72.9 (2), −65.8 (2) and 71.8 (2)°], as well as the orientation of the hy­droxy H atoms. Furthermore, the crystal structure displays two different types of strong hydrogen bond. The first is between an alcohol O—H and another alcohol O atom, and the second between an alcohol O—H group and an ether O atom. Additional weak hydrogen bonds between C—H groups and ether O atoms stabilize the structure. International Union of Crystallography 2013-07-24 /pmc/articles/PMC3793793/ /pubmed/24109380 http://dx.doi.org/10.1107/S1600536813019818 Text en © Meister et al. 2013 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
Meister, Anne C.
Lang, Mathias
Nieger, Martin
Bräse, Stefan
4-(2-Hy­droxy­eth­oxy)phenol
title 4-(2-Hy­droxy­eth­oxy)phenol
title_full 4-(2-Hy­droxy­eth­oxy)phenol
title_fullStr 4-(2-Hy­droxy­eth­oxy)phenol
title_full_unstemmed 4-(2-Hy­droxy­eth­oxy)phenol
title_short 4-(2-Hy­droxy­eth­oxy)phenol
title_sort 4-(2-hy­droxy­eth­oxy)phenol
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3793793/
https://www.ncbi.nlm.nih.gov/pubmed/24109380
http://dx.doi.org/10.1107/S1600536813019818
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AT niegermartin 42hydroxyethoxyphenol
AT brasestefan 42hydroxyethoxyphenol

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