A general synthesis of chromenes, involving zinc promoted allyation of
2-hydroxyphenacyl derivatives followed by acid catalyzed cyclisation
and dehydration is described. Several structurally different allylic b
romides have been successfully employed. The synthesis is conveniently
carried out without isolation of the intermediate benzyl alcohol deri
vative, and usually good overall yields are obtained. Salicyl aldehyde
was successfully employed as a substrate, but precocene was not forme
d from 4,5-dimethoxysalicylaldehyde.