4-(4-Chlorophenyl)piperidin-4-ol

In the title compound, C11H14ClNO, the piperidine ring adopts a chair conformation: the hydroxyl substituent and the N-bound H atom occupy the axial positions, while the benzene ring occupies the equatorial position. In the crystal, the molecules are linked into a centrosymmetric tetramer through st...

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Main Authors: Maciej Kubicki, M. S. Siddegowda, H. S. Yathirajan, B. P. Siddaraju, Grzegorz Dutkiewicz
Format: Article
Language:English
Published: International Union of Crystallography 2010-03-01
Series:Acta Crystallographica Section E
Online Access:http://scripts.iucr.org/cgi-bin/paper?S1600536810004216
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author Maciej Kubicki
M. S. Siddegowda
H. S. Yathirajan
B. P. Siddaraju
Grzegorz Dutkiewicz
author_facet Maciej Kubicki
M. S. Siddegowda
H. S. Yathirajan
B. P. Siddaraju
Grzegorz Dutkiewicz
author_sort Maciej Kubicki
collection DOAJ
description In the title compound, C11H14ClNO, the piperidine ring adopts a chair conformation: the hydroxyl substituent and the N-bound H atom occupy the axial positions, while the benzene ring occupies the equatorial position. In the crystal, the molecules are linked into a centrosymmetric tetramer through strong O—H...N and weak N—H...O hydrogen bonds; the N and O atoms act as both donor and acceptor for these interactions. The tetramers are further joined by hydrogen bonds into a layer parallel to (100).
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spelling doaj.art-999d2036f6754166874c9f4d1a95ed8c2022-12-21T17:24:00ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682010-03-01663o562o56210.1107/S16005368100042164-(4-Chlorophenyl)piperidin-4-olMaciej KubickiM. S. SiddegowdaH. S. YathirajanB. P. SiddarajuGrzegorz DutkiewiczIn the title compound, C11H14ClNO, the piperidine ring adopts a chair conformation: the hydroxyl substituent and the N-bound H atom occupy the axial positions, while the benzene ring occupies the equatorial position. In the crystal, the molecules are linked into a centrosymmetric tetramer through strong O—H...N and weak N—H...O hydrogen bonds; the N and O atoms act as both donor and acceptor for these interactions. The tetramers are further joined by hydrogen bonds into a layer parallel to (100).http://scripts.iucr.org/cgi-bin/paper?S1600536810004216
spellingShingle Maciej Kubicki
M. S. Siddegowda
H. S. Yathirajan
B. P. Siddaraju
Grzegorz Dutkiewicz
4-(4-Chlorophenyl)piperidin-4-ol
Acta Crystallographica Section E
title 4-(4-Chlorophenyl)piperidin-4-ol
title_full 4-(4-Chlorophenyl)piperidin-4-ol
title_fullStr 4-(4-Chlorophenyl)piperidin-4-ol
title_full_unstemmed 4-(4-Chlorophenyl)piperidin-4-ol
title_short 4-(4-Chlorophenyl)piperidin-4-ol
title_sort 4 4 chlorophenyl piperidin 4 ol
url http://scripts.iucr.org/cgi-bin/paper?S1600536810004216
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AT mssiddegowda 44chlorophenylpiperidin4ol
AT hsyathirajan 44chlorophenylpiperidin4ol
AT bpsiddaraju 44chlorophenylpiperidin4ol
AT grzegorzdutkiewicz 44chlorophenylpiperidin4ol