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3-[(E)-1-(Benzyl­oxyimino)eth­yl]-2-oxo-2H-chromen-7-yl acetate

The title compound, C(20)H(17)NO(5), was prepared by the reaction of 3-acetyl-2-oxo-2H-chromen-7-yl acetate with benzyl­oxy­amine. The mol­ecule adopts an E configuration with respect to the C=N double bond. The dihedral angles between the coumarin ring system, the phenyl ring and the C=N—O—C plane...

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Detalles Bibliográficos
Autores principales: Wang, Hui, Xu, Su-hua, Zeng, Zhuo, Zhang, Yong-hong
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983746/
https://www.ncbi.nlm.nih.gov/pubmed/21580286
http://dx.doi.org/10.1107/S1600536810003454
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author Wang, Hui
Xu, Su-hua
Zeng, Zhuo
Zhang, Yong-hong
author_facet Wang, Hui
Xu, Su-hua
Zeng, Zhuo
Zhang, Yong-hong
author_sort Wang, Hui
collection PubMed
description The title compound, C(20)H(17)NO(5), was prepared by the reaction of 3-acetyl-2-oxo-2H-chromen-7-yl acetate with benzyl­oxy­amine. The mol­ecule adopts an E configuration with respect to the C=N double bond. The dihedral angles between the coumarin ring system, the phenyl ring and the C=N—O—C plane of the oxime unit are 35.83 (6), 35.8 (2) and 69.99 (15)°, respectively. In the crystal, a two-dimensional supra­molecular network is assembled through weak inter­molecular C—H⋯O hydrogen-bonding inter­actions.
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spelling pubmed-29837462010-12-30 3-[(E)-1-(Benzyl­oxyimino)eth­yl]-2-oxo-2H-chromen-7-yl acetate Wang, Hui Xu, Su-hua Zeng, Zhuo Zhang, Yong-hong Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(20)H(17)NO(5), was prepared by the reaction of 3-acetyl-2-oxo-2H-chromen-7-yl acetate with benzyl­oxy­amine. The mol­ecule adopts an E configuration with respect to the C=N double bond. The dihedral angles between the coumarin ring system, the phenyl ring and the C=N—O—C plane of the oxime unit are 35.83 (6), 35.8 (2) and 69.99 (15)°, respectively. In the crystal, a two-dimensional supra­molecular network is assembled through weak inter­molecular C—H⋯O hydrogen-bonding inter­actions. International Union of Crystallography 2010-02-03 /pmc/articles/PMC2983746/ /pubmed/21580286 http://dx.doi.org/10.1107/S1600536810003454 Text en © Wang et al. 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
Wang, Hui
Xu, Su-hua
Zeng, Zhuo
Zhang, Yong-hong
3-[(E)-1-(Benzyl­oxyimino)eth­yl]-2-oxo-2H-chromen-7-yl acetate
title 3-[(E)-1-(Benzyl­oxyimino)eth­yl]-2-oxo-2H-chromen-7-yl acetate
title_full 3-[(E)-1-(Benzyl­oxyimino)eth­yl]-2-oxo-2H-chromen-7-yl acetate
title_fullStr 3-[(E)-1-(Benzyl­oxyimino)eth­yl]-2-oxo-2H-chromen-7-yl acetate
title_full_unstemmed 3-[(E)-1-(Benzyl­oxyimino)eth­yl]-2-oxo-2H-chromen-7-yl acetate
title_short 3-[(E)-1-(Benzyl­oxyimino)eth­yl]-2-oxo-2H-chromen-7-yl acetate
title_sort 3-[(e)-1-(benzyl­oxyimino)eth­yl]-2-oxo-2h-chromen-7-yl acetate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983746/
https://www.ncbi.nlm.nih.gov/pubmed/21580286
http://dx.doi.org/10.1107/S1600536810003454
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