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...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
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International Union of Crystallography
2010-03-01
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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). |
first_indexed | 2024-12-24T00:39:38Z |
format | Article |
id | doaj.art-999d2036f6754166874c9f4d1a95ed8c |
institution | Directory Open Access Journal |
issn | 1600-5368 |
language | English |
last_indexed | 2024-12-24T00:39:38Z |
publishDate | 2010-03-01 |
publisher | International Union of Crystallography |
record_format | Article |
series | Acta Crystallographica Section E |
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 |
work_keys_str_mv | AT maciejkubicki 44chlorophenylpiperidin4ol AT mssiddegowda 44chlorophenylpiperidin4ol AT hsyathirajan 44chlorophenylpiperidin4ol AT bpsiddaraju 44chlorophenylpiperidin4ol AT grzegorzdutkiewicz 44chlorophenylpiperidin4ol |