Research Article: 2-Cyclo­hexyl-4-methyl­tetra­hydro­pyran-4-ol1

Date Published: May 01, 2010

Publisher: International Union of Crystallography

Author(s): Edward R. T. Tiekink, Alexandra Macedo, Edison P. Wendler, Alcindo A. Dos Santos, Julio Zukerman-Schpector.

http://doi.org/10.1107/S1600536810015333

Abstract

In the title compound, C12H22O2, the 4-methyl­tetra­hydro­pyran-4-ol ring adopts a conformation close to that of a chair and with the two O atoms syn; the cyclo­hexyl group occupies an equatorial position and adopts a chair conformation. In the crystal packing, supra­molecular chains along the b axis are sustained by O—H⋯O hydrogen bonds. These are connected into undulating layers in the ab plane by C—H⋯O inter­actions.

Partial Text

For background to the solvent-free catalysed synthesis of tetra­hydro­pyran odorants, see: Macedo et al. (2010 ▶). For conformational analysis, see: Cremer & Pople (1975 ▶)

 

Source:

http://doi.org/10.1107/S1600536810015333

 

0 0 vote
Article Rating
Subscribe
Notify of
guest
0 Comments
Inline Feedbacks
View all comments