Alkylation of phenol, anisole, and their methyl-substituted derivative with
camphene catalyzed by large-porous beta-zeolite yielded the corresponding
terpenylphenols, terpenylanisoles, and terpenyl phenyl ethers. C- or O-alky
iation occurs depending on phenol structure and on the solvent used. At C-a
lkylation the main reaction product has uncommon structure of the terpene r
est with methyl groups in 1, 4,and 7 positions.