Reaction of nitroarenes with phenylthiomethyl isocyanide in the presence of potassium tert-butoxide results in the introduction of the isocyanomethyl substituent into positions ortho or para to the nitro group. The products of the reaction when subjected to mild hydrolysis can be converted into nitrobenzylic amines or their formyl derivatives.
硝基
芳烃与
苯硫甲基异氰酸酯在四
氟化
钾存在下反应,导致异
氰甲基取代基引入到硝基组的邻位或对位。该反应的产物经过温和
水解后可转化为硝基
苄胺或其甲酰衍
生物。