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The title compound, C 11 H 14 Cl 2 O, 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.

(5R)-5-[(1R)-2,2-Dichloro-1-methylcyclopropyl]-2-methylcyclohex-2-en-1-one