The reduction of coumarin, 4-methylcoumarin, 2,2-dimethyl-2H-chromene
and 2,2,4-trimethyl-2H-chromene with sodium or lithium in liquid ammon
ia with the presence or without donor of protons was carried out. The
formation of phenolic products was observed when a limited amount of a
lcohol as a proton donor was present in the reaction medium. In the ex
periments with excess of alcohol the products with a partially reduced
benzene ring were formed.