2,2′-[(2S*,6R*)-Piperidine-2,6-di­yl]­di­pro­pan-2-ol

In the title compound, C(11)H(23)NO(2), the piperidine ring has a chair conformation. The two hy­droxy H atoms are disordered over two positions with fixed occupancy ratios of 0.57:0.43 and 0.63:0.37. In the mol­ecule, there are two short N—H⋯O inter­actions. In the crystal, four symmetry-related mo...

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Detalles Bibliográficos
Autores principales: Journot, Guillaume, Neier, Reinhard, Stoeckli-Evans, Helen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3297911/
https://www.ncbi.nlm.nih.gov/pubmed/22412714
http://dx.doi.org/10.1107/S1600536812005879
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author Journot, Guillaume
Neier, Reinhard
Stoeckli-Evans, Helen
author_facet Journot, Guillaume
Neier, Reinhard
Stoeckli-Evans, Helen
author_sort Journot, Guillaume
collection PubMed
description In the title compound, C(11)H(23)NO(2), the piperidine ring has a chair conformation. The two hy­droxy H atoms are disordered over two positions with fixed occupancy ratios of 0.57:0.43 and 0.63:0.37. In the mol­ecule, there are two short N—H⋯O inter­actions. In the crystal, four symmetry-related mol­ecules are linked by O—H⋯O hydrogen bonds to form a cage-like arrangement, centered about the point of inter­section of three twofold axes. These cages stack along the [100] direction.
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spelling pubmed-32979112012-03-12 2,2′-[(2S*,6R*)-Piperidine-2,6-di­yl]­di­pro­pan-2-ol Journot, Guillaume Neier, Reinhard Stoeckli-Evans, Helen Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(11)H(23)NO(2), the piperidine ring has a chair conformation. The two hy­droxy H atoms are disordered over two positions with fixed occupancy ratios of 0.57:0.43 and 0.63:0.37. In the mol­ecule, there are two short N—H⋯O inter­actions. In the crystal, four symmetry-related mol­ecules are linked by O—H⋯O hydrogen bonds to form a cage-like arrangement, centered about the point of inter­section of three twofold axes. These cages stack along the [100] direction. International Union of Crystallography 2012-02-24 /pmc/articles/PMC3297911/ /pubmed/22412714 http://dx.doi.org/10.1107/S1600536812005879 Text en © Journot 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
Journot, Guillaume
Neier, Reinhard
Stoeckli-Evans, Helen
2,2′-[(2S*,6R*)-Piperidine-2,6-di­yl]­di­pro­pan-2-ol
title 2,2′-[(2S*,6R*)-Piperidine-2,6-di­yl]­di­pro­pan-2-ol
title_full 2,2′-[(2S*,6R*)-Piperidine-2,6-di­yl]­di­pro­pan-2-ol
title_fullStr 2,2′-[(2S*,6R*)-Piperidine-2,6-di­yl]­di­pro­pan-2-ol
title_full_unstemmed 2,2′-[(2S*,6R*)-Piperidine-2,6-di­yl]­di­pro­pan-2-ol
title_short 2,2′-[(2S*,6R*)-Piperidine-2,6-di­yl]­di­pro­pan-2-ol
title_sort 2,2′-[(2s*,6r*)-piperidine-2,6-di­yl]­di­pro­pan-2-ol
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3297911/
https://www.ncbi.nlm.nih.gov/pubmed/22412714
http://dx.doi.org/10.1107/S1600536812005879
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