Acta Cryst. (2005). E61, o2395-o2397  [ doi:10.1107/S1600536805020222 ]

Racemic trans-4-phenylperhydropyran-3-ol

J. Hartung, I. Svoboda, P. Schmidt and H. Fuess

Abstract: In the title compound, C₁₁H₁₄O₂, the tetrahydropyran ring adopts a ¹C₄ conformation, with the phenyl and the hydroxy substituents located in equatorial positions. Hydrogen bonding occurs in the solid state between hydroxy groups to link two molecules of (R,R)-trans-4-phenylperhydropyran-3-ol and two molecules of the (S,S)-enantiomer to provide tetramers.

Online 6 July 2005

Copyright © International Union of Crystallography
IUCr Webmaster