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Diethyl 2,2-bis­(3,5-di-tert-butyl-4-hy­droxy­benz­yl)malonate

The title mol­ecule, C(37)H(56)O(6), possesses twofold symmetry, with the twofold axis passing through the quaternary C atom. In the crystal, neighbouring mol­ecules are linked via O—H⋯O hydrogen bonds involving the phenol OH group and the carbonyl O atom, forming chains propagating in [101]. Within...

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Detalles Bibliográficos
Autores principales: Zeng, Tao, Hou, Yu-Ping, Ren, Wan-Zhong, Xu, Wen-You
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275203/
https://www.ncbi.nlm.nih.gov/pubmed/22347059
http://dx.doi.org/10.1107/S1600536811054900
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author Zeng, Tao
Hou, Yu-Ping
Ren, Wan-Zhong
Xu, Wen-You
author_facet Zeng, Tao
Hou, Yu-Ping
Ren, Wan-Zhong
Xu, Wen-You
author_sort Zeng, Tao
collection PubMed
description The title mol­ecule, C(37)H(56)O(6), possesses twofold symmetry, with the twofold axis passing through the quaternary C atom. In the crystal, neighbouring mol­ecules are linked via O—H⋯O hydrogen bonds involving the phenol OH group and the carbonyl O atom, forming chains propagating in [101]. Within these chains, rings are formed with an R (2) (2)(20) motif. There are also C—H⋯O inter­actions present within the rings.
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spelling pubmed-32752032012-02-15 Diethyl 2,2-bis­(3,5-di-tert-butyl-4-hy­droxy­benz­yl)malonate Zeng, Tao Hou, Yu-Ping Ren, Wan-Zhong Xu, Wen-You Acta Crystallogr Sect E Struct Rep Online Organic Papers The title mol­ecule, C(37)H(56)O(6), possesses twofold symmetry, with the twofold axis passing through the quaternary C atom. In the crystal, neighbouring mol­ecules are linked via O—H⋯O hydrogen bonds involving the phenol OH group and the carbonyl O atom, forming chains propagating in [101]. Within these chains, rings are formed with an R (2) (2)(20) motif. There are also C—H⋯O inter­actions present within the rings. International Union of Crystallography 2012-01-18 /pmc/articles/PMC3275203/ /pubmed/22347059 http://dx.doi.org/10.1107/S1600536811054900 Text en © Zeng 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
Zeng, Tao
Hou, Yu-Ping
Ren, Wan-Zhong
Xu, Wen-You
Diethyl 2,2-bis­(3,5-di-tert-butyl-4-hy­droxy­benz­yl)malonate
title Diethyl 2,2-bis­(3,5-di-tert-butyl-4-hy­droxy­benz­yl)malonate
title_full Diethyl 2,2-bis­(3,5-di-tert-butyl-4-hy­droxy­benz­yl)malonate
title_fullStr Diethyl 2,2-bis­(3,5-di-tert-butyl-4-hy­droxy­benz­yl)malonate
title_full_unstemmed Diethyl 2,2-bis­(3,5-di-tert-butyl-4-hy­droxy­benz­yl)malonate
title_short Diethyl 2,2-bis­(3,5-di-tert-butyl-4-hy­droxy­benz­yl)malonate
title_sort diethyl 2,2-bis­(3,5-di-tert-butyl-4-hy­droxy­benz­yl)malonate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275203/
https://www.ncbi.nlm.nih.gov/pubmed/22347059
http://dx.doi.org/10.1107/S1600536811054900
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