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(4-Hydr­oxy-2,5-dimethyl­phen­yl)phenyl­methanone

The title compound, C(15)H(14)O(2), was obtained by Friedel–Crafts acyl­ation between 2,5-dimethyl­phenol and benzoyl chloride in the presence of aluminium chloride as a catalyst. The dihedral angle between the benzene rings is 61.95 (4)°. In the crystal, O—H⋯O hydrogen bonding and C—H⋯O weak inter­...

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Detalles Bibliográficos
Autores principales: Moreno-Fuquen, Rodolfo, Valencia, Leidy J., Kennedy, Alan R., Gilmour, Denise, De Almeida Santos, R. H.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971310/
https://www.ncbi.nlm.nih.gov/pubmed/21578230
http://dx.doi.org/10.1107/S1600536809039488
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author Moreno-Fuquen, Rodolfo
Valencia, Leidy J.
Kennedy, Alan R.
Gilmour, Denise
De Almeida Santos, R. H.
author_facet Moreno-Fuquen, Rodolfo
Valencia, Leidy J.
Kennedy, Alan R.
Gilmour, Denise
De Almeida Santos, R. H.
author_sort Moreno-Fuquen, Rodolfo
collection PubMed
description The title compound, C(15)H(14)O(2), was obtained by Friedel–Crafts acyl­ation between 2,5-dimethyl­phenol and benzoyl chloride in the presence of aluminium chloride as a catalyst. The dihedral angle between the benzene rings is 61.95 (4)°. In the crystal, O—H⋯O hydrogen bonding and C—H⋯O weak inter­actions lead to polymeric C(6), C(8) and C(11) chains along the a, b and c-axis directions, respectively.
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spelling pubmed-29713102010-12-30 (4-Hydr­oxy-2,5-dimethyl­phen­yl)phenyl­methanone Moreno-Fuquen, Rodolfo Valencia, Leidy J. Kennedy, Alan R. Gilmour, Denise De Almeida Santos, R. H. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(15)H(14)O(2), was obtained by Friedel–Crafts acyl­ation between 2,5-dimethyl­phenol and benzoyl chloride in the presence of aluminium chloride as a catalyst. The dihedral angle between the benzene rings is 61.95 (4)°. In the crystal, O—H⋯O hydrogen bonding and C—H⋯O weak inter­actions lead to polymeric C(6), C(8) and C(11) chains along the a, b and c-axis directions, respectively. International Union of Crystallography 2009-10-03 /pmc/articles/PMC2971310/ /pubmed/21578230 http://dx.doi.org/10.1107/S1600536809039488 Text en © Moreno-Fuquen et al. 2009 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
Moreno-Fuquen, Rodolfo
Valencia, Leidy J.
Kennedy, Alan R.
Gilmour, Denise
De Almeida Santos, R. H.
(4-Hydr­oxy-2,5-dimethyl­phen­yl)phenyl­methanone
title (4-Hydr­oxy-2,5-dimethyl­phen­yl)phenyl­methanone
title_full (4-Hydr­oxy-2,5-dimethyl­phen­yl)phenyl­methanone
title_fullStr (4-Hydr­oxy-2,5-dimethyl­phen­yl)phenyl­methanone
title_full_unstemmed (4-Hydr­oxy-2,5-dimethyl­phen­yl)phenyl­methanone
title_short (4-Hydr­oxy-2,5-dimethyl­phen­yl)phenyl­methanone
title_sort (4-hydr­oxy-2,5-dimethyl­phen­yl)phenyl­methanone
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971310/
https://www.ncbi.nlm.nih.gov/pubmed/21578230
http://dx.doi.org/10.1107/S1600536809039488
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