Acta Crystallographica Section E (Jul 2011)
(5R)-5-[(1R)-2,2-Dichloro-1-methylcyclopropyl]-2-methylcyclohex-2-en-1-one
Abstract
The title compound, C11H14Cl2O, was synthesized by the reaction of a dichloromethane solution of (R)-carvone and potassium tert-butanolate in the presence of a catalytic amount of benzyltriethylammonium chloride in chloroform. The cyclohexene ring adopts a half-boat conformation. The cyclopropyl ring is unsymmetrical, the shortest C—C bond being distal to the alkyl-substituted C atom. The crystal packing is stabilized only by van der Waals interactions.