(2S,3S)-2,6-dimethylheptane-1,3-diol, the oxygenated side chain of 22(S)-hydroxycholestrol, and its synthetic precursor (R)-4-benzyl-3-[(2R,3S)-3-hydroxy-2,6-dimethylheptanoyl]-1,3-oxazolidin-2-one

Acta Crystallogr C. 2013 Jun;69(Pt 6):647-50. doi: 10.1107/S0108270113011852. Epub 2013 May 15.

Abstract

(2S,3S)-2,6-dimethylheptane-1,3-diol, C9H20O2, (I), was synthesized from the ketone (R)-4-benzyl-3-[(2R,3S)-3-hydroxy-2,6-dimethylheptanoyl]-1,3-oxazolidin-2-one, C19H27NO4, (II), containing C atoms of known chirality. In both structures, strong hydrogen bonds between the hydroxy groups form tape motifs. The contribution from weaker C-H···O hydrogen bonds is much more evident in the structure of (II), which furthermore contains an example of a direct short Osp(3)···Csp(2) contact that represents a usually unrecognized type of intermolecular interaction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chemistry Techniques, Synthetic
  • Crystallography, X-Ray
  • Glycols / chemical synthesis
  • Glycols / chemistry*
  • Hydrogen Bonding
  • Hydroxycholesterols / chemistry*
  • Molecular Conformation
  • Molecular Structure
  • Oxazolidinones / chemistry
  • Stereoisomerism

Substances

  • Glycols
  • Hydroxycholesterols
  • Oxazolidinones
  • 22-hydroxycholesterol