[2,5-Bis(di­propyl­amino)-4-(hy­droxy­meth­yl)phen­yl]methanol

The centrosymmetric title compound, C(22)H(36)N(2)O(2), was prepared in five steps from diethyl succinate. The di­propyl­amino groups are almost orthogonal to the central phenyl­enedi­methanol ring [dihedral angle = 87.62 (9)°]. In the crystal, the mol­ecules are connected by O—H⋯N hydrogen bonds, f...

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Detalles Bibliográficos
Autores principales: Schmitt, Volker, Holzmann, Gideon, Schollmeyer, Dieter, Detert, Heiner
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2021
Materias:
Data Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462325/
https://www.ncbi.nlm.nih.gov/pubmed/36339103
http://dx.doi.org/10.1107/S2414314621004430
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author Schmitt, Volker
Holzmann, Gideon
Schollmeyer, Dieter
Detert, Heiner
author_facet Schmitt, Volker
Holzmann, Gideon
Schollmeyer, Dieter
Detert, Heiner
author_sort Schmitt, Volker
collection PubMed
description The centrosymmetric title compound, C(22)H(36)N(2)O(2), was prepared in five steps from diethyl succinate. The di­propyl­amino groups are almost orthogonal to the central phenyl­enedi­methanol ring [dihedral angle = 87.62 (9)°]. In the crystal, the mol­ecules are connected by O—H⋯N hydrogen bonds, forming (101) layers separated by the propyl chains. [Image: see text]
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spelling pubmed-94623252022-11-04 [2,5-Bis(di­propyl­amino)-4-(hy­droxy­meth­yl)phen­yl]methanol Schmitt, Volker Holzmann, Gideon Schollmeyer, Dieter Detert, Heiner IUCrdata Data Reports The centrosymmetric title compound, C(22)H(36)N(2)O(2), was prepared in five steps from diethyl succinate. The di­propyl­amino groups are almost orthogonal to the central phenyl­enedi­methanol ring [dihedral angle = 87.62 (9)°]. In the crystal, the mol­ecules are connected by O—H⋯N hydrogen bonds, forming (101) layers separated by the propyl chains. [Image: see text] International Union of Crystallography 2021-04-30 /pmc/articles/PMC9462325/ /pubmed/36339103 http://dx.doi.org/10.1107/S2414314621004430 Text en © Schmitt et al. 2021 https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Data Reports
Schmitt, Volker
Holzmann, Gideon
Schollmeyer, Dieter
Detert, Heiner
[2,5-Bis(di­propyl­amino)-4-(hy­droxy­meth­yl)phen­yl]methanol
title [2,5-Bis(di­propyl­amino)-4-(hy­droxy­meth­yl)phen­yl]methanol
title_full [2,5-Bis(di­propyl­amino)-4-(hy­droxy­meth­yl)phen­yl]methanol
title_fullStr [2,5-Bis(di­propyl­amino)-4-(hy­droxy­meth­yl)phen­yl]methanol
title_full_unstemmed [2,5-Bis(di­propyl­amino)-4-(hy­droxy­meth­yl)phen­yl]methanol
title_short [2,5-Bis(di­propyl­amino)-4-(hy­droxy­meth­yl)phen­yl]methanol
title_sort [2,5-bis(di­propyl­amino)-4-(hy­droxy­meth­yl)phen­yl]methanol
topic Data Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462325/
https://www.ncbi.nlm.nih.gov/pubmed/36339103
http://dx.doi.org/10.1107/S2414314621004430
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AT detertheiner 25bisdipropylamino4hydroxymethylphenylmethanol

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