Abstract
Treatment of salicylidene-anils with potassium cyanide in acetic acid affords 1:1 adducts shown to be the hydrocyano derivatives. When the reaction is conducted in alcohol, salicylidene derivatives of 2-amino-3-arylaminobenzofurans or α-arylamino-o-hydroxyphenylacetamides are formed depending on the molar ratio of the reactants. The formation of the products and the previously reported structures are discussed.
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