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Diethyl 4,4′-(3,6-dioxaoctane-1,8-diyl­dioxy)dibenzoate

The title compound, C(24)H(30)O(8), was obtained by reaction of ethyl 4-hy­droxy­benzoate with 1,2-dichloro­ethane. The mol­ecule occupies a crystallographic inversion center, with its central ethyl­ene bridge in an anti conformation. The other ethyl­ene bridge has a gauche conformation, with the co...

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Detalles Bibliográficos
Autores principales: Ma, Zhen, Qin, Haisha, Lai, Gang, Fan, Jingjie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3295487/
https://www.ncbi.nlm.nih.gov/pubmed/22412598
http://dx.doi.org/10.1107/S1600536812004874
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author Ma, Zhen
Qin, Haisha
Lai, Gang
Fan, Jingjie
author_facet Ma, Zhen
Qin, Haisha
Lai, Gang
Fan, Jingjie
author_sort Ma, Zhen
collection PubMed
description The title compound, C(24)H(30)O(8), was obtained by reaction of ethyl 4-hy­droxy­benzoate with 1,2-dichloro­ethane. The mol­ecule occupies a crystallographic inversion center, with its central ethyl­ene bridge in an anti conformation. The other ethyl­ene bridge has a gauche conformation, with the corresponding O—C—C—O torsion angle being 74.2 (1)°. The benzene rings are almost coplanar with the adjacent eth­oxy­carbonyl groups, with an r.m.s. deviation of 0.078 Å.
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spelling pubmed-32954872012-03-12 Diethyl 4,4′-(3,6-dioxaoctane-1,8-diyl­dioxy)dibenzoate Ma, Zhen Qin, Haisha Lai, Gang Fan, Jingjie Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(24)H(30)O(8), was obtained by reaction of ethyl 4-hy­droxy­benzoate with 1,2-dichloro­ethane. The mol­ecule occupies a crystallographic inversion center, with its central ethyl­ene bridge in an anti conformation. The other ethyl­ene bridge has a gauche conformation, with the corresponding O—C—C—O torsion angle being 74.2 (1)°. The benzene rings are almost coplanar with the adjacent eth­oxy­carbonyl groups, with an r.m.s. deviation of 0.078 Å. International Union of Crystallography 2012-02-17 /pmc/articles/PMC3295487/ /pubmed/22412598 http://dx.doi.org/10.1107/S1600536812004874 Text en © Ma 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
Ma, Zhen
Qin, Haisha
Lai, Gang
Fan, Jingjie
Diethyl 4,4′-(3,6-dioxaoctane-1,8-diyl­dioxy)dibenzoate
title Diethyl 4,4′-(3,6-dioxaoctane-1,8-diyl­dioxy)dibenzoate
title_full Diethyl 4,4′-(3,6-dioxaoctane-1,8-diyl­dioxy)dibenzoate
title_fullStr Diethyl 4,4′-(3,6-dioxaoctane-1,8-diyl­dioxy)dibenzoate
title_full_unstemmed Diethyl 4,4′-(3,6-dioxaoctane-1,8-diyl­dioxy)dibenzoate
title_short Diethyl 4,4′-(3,6-dioxaoctane-1,8-diyl­dioxy)dibenzoate
title_sort diethyl 4,4′-(3,6-dioxaoctane-1,8-diyl­dioxy)dibenzoate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3295487/
https://www.ncbi.nlm.nih.gov/pubmed/22412598
http://dx.doi.org/10.1107/S1600536812004874
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