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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...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2009
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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. |
format | Text |
id | pubmed-2971310 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT morenofuquenrodolfo 4hydroxy25dimethylphenylphenylmethanone AT valencialeidyj 4hydroxy25dimethylphenylphenylmethanone AT kennedyalanr 4hydroxy25dimethylphenylphenylmethanone AT gilmourdenise 4hydroxy25dimethylphenylphenylmethanone AT dealmeidasantosrh 4hydroxy25dimethylphenylphenylmethanone |