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N-Benzyl-2-(3-chloro-4-hydroxyphenyl)acetamide
The title compound, C(15)H(14)ClNO(2), was synthesized as part of a project to generate a combinatorial library based on the fungal natural product 2-(3-chloro-4-hydroxyphenyl)acetamide. It crystallizes as non-planar discrete molecules [the peripheral 3-chloro-4-hydroxyphenyl and benzyl groups...
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983291/ https://www.ncbi.nlm.nih.gov/pubmed/21587515 http://dx.doi.org/10.1107/S1600536810035397 |
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author | Davis, Rohan A. Healy, Peter C. |
author_facet | Davis, Rohan A. Healy, Peter C. |
author_sort | Davis, Rohan A. |
collection | PubMed |
description | The title compound, C(15)H(14)ClNO(2), was synthesized as part of a project to generate a combinatorial library based on the fungal natural product 2-(3-chloro-4-hydroxyphenyl)acetamide. It crystallizes as non-planar discrete molecules [the peripheral 3-chloro-4-hydroxyphenyl and benzyl groups are twisted out of the plane of the central acetamide group, with N—C—C—C and C—C—C—C torsion angles of −58.8 (3) and 65.0 (2)°, respectively] linked by intermolecular N—H⋯O and O—H⋯O hydrogen bonds. |
format | Text |
id | pubmed-2983291 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29832912010-12-30 N-Benzyl-2-(3-chloro-4-hydroxyphenyl)acetamide Davis, Rohan A. Healy, Peter C. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(15)H(14)ClNO(2), was synthesized as part of a project to generate a combinatorial library based on the fungal natural product 2-(3-chloro-4-hydroxyphenyl)acetamide. It crystallizes as non-planar discrete molecules [the peripheral 3-chloro-4-hydroxyphenyl and benzyl groups are twisted out of the plane of the central acetamide group, with N—C—C—C and C—C—C—C torsion angles of −58.8 (3) and 65.0 (2)°, respectively] linked by intermolecular N—H⋯O and O—H⋯O hydrogen bonds. International Union of Crystallography 2010-09-08 /pmc/articles/PMC2983291/ /pubmed/21587515 http://dx.doi.org/10.1107/S1600536810035397 Text en © Davis and Healy 2010 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 Davis, Rohan A. Healy, Peter C. N-Benzyl-2-(3-chloro-4-hydroxyphenyl)acetamide |
title |
N-Benzyl-2-(3-chloro-4-hydroxyphenyl)acetamide |
title_full |
N-Benzyl-2-(3-chloro-4-hydroxyphenyl)acetamide |
title_fullStr |
N-Benzyl-2-(3-chloro-4-hydroxyphenyl)acetamide |
title_full_unstemmed |
N-Benzyl-2-(3-chloro-4-hydroxyphenyl)acetamide |
title_short |
N-Benzyl-2-(3-chloro-4-hydroxyphenyl)acetamide |
title_sort | n-benzyl-2-(3-chloro-4-hydroxyphenyl)acetamide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983291/ https://www.ncbi.nlm.nih.gov/pubmed/21587515 http://dx.doi.org/10.1107/S1600536810035397 |
work_keys_str_mv | AT davisrohana nbenzyl23chloro4hydroxyphenylacetamide AT healypeterc nbenzyl23chloro4hydroxyphenylacetamide |