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(E)-(2,4-Dichloro-phen-yl)[2-hydr-oxy-6-(methoxy-imino)cyclo-hex-1-en-yl]methanone.

ABSTRACT: The title compound, C(14)H(13)Cl(2)NO(3), was obtained as the product of an attempted synthesis of herbicidally active compounds containing oxime ether and cyclo-hexenone groups. In the crystal structure, the mol-ecule adopts an endocyclic enol tautomeric form and the cyclo-hexene ring adopts a distorted envelope form. The oxime ether group has an E configuration, with the meth-oxy group anti to the ortho-chloro substitutent. Intra-molecular O-H?O and inter-molecular C-H?O hydrogen bonds are found in the crystal structure.

SUBMITTER: Huang GD 

PROVIDER: S-EPMC2968194 | biostudies-literature | 2009 Jan

REPOSITORIES: biostudies-literature

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(E)-(2,4-Dichloro-phen-yl)[2-hydr-oxy-6-(methoxy-imino)cyclo-hex-1-en-yl]methanone.

Huang Guang-Dong GD   Zou Jian-Wei JW   Zhao Wen-Na WN   Zhao Shu-Min SM  

Acta crystallographica. Section E, Structure reports online 20090123 Pt 2

The title compound, C(14)H(13)Cl(2)NO(3), was obtained as the product of an attempted synthesis of herbicidally active compounds containing oxime ether and cyclo-hexenone groups. In the crystal structure, the mol-ecule adopts an endocyclic enol tautomeric form and the cyclo-hexene ring adopts a distorted envelope form. The oxime ether group has an E configuration, with the meth-oxy group anti to the ortho-chloro substitutent. Intra-molecular O-H⋯O and inter-molecular C-H⋯O hydrogen bonds are fou  ...[more]

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