Abstract
In the title compound, C12H13ClO4, the 1,3-dioxane ring adopts a chair conformation and the 2-chlorobenzene and methyl substituents occupy equatorial sites. The carboxyl group is in an axial inclination. In the crystal, carboxylic acid inversion dimers linked by pairs of O—H⋯O hydrogen bonds generate R 2 2(8) loops.
Highlights
In the title compound, C12H13ClO4, the 1,3-dioxane ring adopts a chair conformation and the 2-chlorobenzene and methyl substituents occupy equatorial sites
The carboxyl group is in an axial inclination
Carboxylic acid inversion dimers linked by pairs of O—H O hydrogen bonds generate R22(8) loops
Summary
Republic of China, and bDepartment of Biology and Chemistry, Hunan University of Science and Engineering, Yongzhou Hunan 425100, People’s Republic of China. H atoms treated by a mixture of independent and constrained refinement max = 0.33 e Å3. R factor = 0.033; wR factor = 0.084; data-to-parameter ratio = 13.2. C12H13ClO4, the 1,3-dioxane ring adopts a chair conformation and the 2-chlorobenzene and methyl substituents occupy equatorial sites. The carboxyl group is in an axial inclination. Carboxylic acid inversion dimers linked by pairs of O—H O hydrogen bonds generate R22(8) loops
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