2-(4-Chloro-phen-yl)-1,3-dioxane - localization of hydrogen atoms
Eric Cyriel Hosten1, Richard Betz1
1Nelson Mandela University, Summerstrand Campus, Department of Chemistry, University Way, Summerstrand, PO Box 77000, Port Elizabeth, 6031, South Africa.
This study details a novel acetal-protected derivative of 4-chloro-benzaldehyde. The compound
Area of Science:
- Organic chemistry
- Crystallography
Background:
- 4-chloro-benzaldehyde derivatives are important in organic synthesis.
- Acetal protection is a common strategy in organic chemistry.
Purpose of the Study:
- To synthesize and characterize a novel acetal-protected derivative of 4-chloro-benzaldehyde.
- To investigate the solid-state structure and intermolecular interactions of the compound.
Main Methods:
- Chemical synthesis of the title compound.
- Single-crystal X-ray diffraction analysis to determine molecular and crystal structure.
Main Results:
- The compound C10H11ClO2 was successfully synthesized.
- The aliphatic ring adopts a chair conformation.
- Molecules form centrosymmetric dimers through weak C-H⋯O hydrogen bonds in the crystal.
Conclusions:
- The study provides a detailed structural characterization of a new 4-chloro-benzaldehyde derivative.
- The observed crystal packing highlights the role of weak interactions in supramolecular assembly.
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