The stereochemistry of the minor isomer, 3,5,5,9-tetramethyldecahydro-
1H-benzocycloheptene, C15H24O2, resulting from the epoxidation of beta
-himachalene has been established. The atoms C10 and the gem-dimethyl
groups C14 and C15 adopt two positions leading to two conformations fo
r the seven-membered ring, boat-shaped (occupation factor 70%) and cha
ir-shaped (30%). Modelling of these conformations agrees with the stat
istical distribution in the crystal.