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(2R*,6S*)-tert-Butyl 2,6-bis­(hydroxy­meth­yl)morpholine-4-carboxyl­ate

In the title compound, C(11)H(21)NO(5), the H atoms of the hydr­oxy groups are disordered over two positions, each in a 1:1 ratio. In the crystal, inter­molecular O—H⋯O hydrogen bonds link pairs of mol­ecules into centrosymmetric dimers. Weak inter­molecular O—H⋯O inter­actions further link these di...

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Detalles Bibliográficos
Autores principales: Chen, Qian, Li, Bojun, Xia, Guangxin
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3006686/
https://www.ncbi.nlm.nih.gov/pubmed/21587854
http://dx.doi.org/10.1107/S1600536810017599
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author Chen, Qian
Li, Bojun
Xia, Guangxin
author_facet Chen, Qian
Li, Bojun
Xia, Guangxin
author_sort Chen, Qian
collection PubMed
description In the title compound, C(11)H(21)NO(5), the H atoms of the hydr­oxy groups are disordered over two positions, each in a 1:1 ratio. In the crystal, inter­molecular O—H⋯O hydrogen bonds link pairs of mol­ecules into centrosymmetric dimers. Weak inter­molecular O—H⋯O inter­actions further link these dimers into chains extended in the [100] direction.
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spelling pubmed-30066862010-12-30 (2R*,6S*)-tert-Butyl 2,6-bis­(hydroxy­meth­yl)morpholine-4-carboxyl­ate Chen, Qian Li, Bojun Xia, Guangxin Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(11)H(21)NO(5), the H atoms of the hydr­oxy groups are disordered over two positions, each in a 1:1 ratio. In the crystal, inter­molecular O—H⋯O hydrogen bonds link pairs of mol­ecules into centrosymmetric dimers. Weak inter­molecular O—H⋯O inter­actions further link these dimers into chains extended in the [100] direction. International Union of Crystallography 2010-06-16 /pmc/articles/PMC3006686/ /pubmed/21587854 http://dx.doi.org/10.1107/S1600536810017599 Text en © Chen et al. 2010 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
Chen, Qian
Li, Bojun
Xia, Guangxin
(2R*,6S*)-tert-Butyl 2,6-bis­(hydroxy­meth­yl)morpholine-4-carboxyl­ate
title (2R*,6S*)-tert-Butyl 2,6-bis­(hydroxy­meth­yl)morpholine-4-carboxyl­ate
title_full (2R*,6S*)-tert-Butyl 2,6-bis­(hydroxy­meth­yl)morpholine-4-carboxyl­ate
title_fullStr (2R*,6S*)-tert-Butyl 2,6-bis­(hydroxy­meth­yl)morpholine-4-carboxyl­ate
title_full_unstemmed (2R*,6S*)-tert-Butyl 2,6-bis­(hydroxy­meth­yl)morpholine-4-carboxyl­ate
title_short (2R*,6S*)-tert-Butyl 2,6-bis­(hydroxy­meth­yl)morpholine-4-carboxyl­ate
title_sort (2r*,6s*)-tert-butyl 2,6-bis­(hydroxy­meth­yl)morpholine-4-carboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3006686/
https://www.ncbi.nlm.nih.gov/pubmed/21587854
http://dx.doi.org/10.1107/S1600536810017599
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