4-(4-Chloro-phen-yl)piperidin-4-ol.
Identifieur interne : 001F76 ( PubMed/Corpus ); précédent : 001F75; suivant : 001F774-(4-Chloro-phen-yl)piperidin-4-ol.
Auteurs : Grzegorz Dutkiewicz ; B P Siddaraju ; H S Yathirajan ; M S Siddegowda ; Maciej KubickiSource :
- Acta crystallographica. Section E, Structure reports online [ 1600-5368 ] ; 2010.
Abstract
In the title compound, C(11)H(14)ClNO, 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 mol-ecules are linked into a centrosymmetric tetra-mer 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 inter-actions. The tetra-mers are further joined by hydrogen bonds into a layer parallel to (100).
DOI: 10.1107/S1600536810004216
PubMed: 21580330
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pubmed:21580330Le document en format XML
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<front><div type="abstract" xml:lang="en">In the title compound, C(11)H(14)ClNO, 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 mol-ecules are linked into a centrosymmetric tetra-mer 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 inter-actions. The tetra-mers are further joined by hydrogen bonds into a layer parallel to (100).</div>
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<Abstract><AbstractText>In the title compound, C(11)H(14)ClNO, 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 mol-ecules are linked into a centrosymmetric tetra-mer 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 inter-actions. The tetra-mers are further joined by hydrogen bonds into a layer parallel to (100).</AbstractText>
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