Racemic trans-4-phen­ylperhydro­pyran-3-ol

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.