Synthesis of Amino and Hydroxy Derivatives of 4,7-Phenanthroline
摘要:
Nitro-, dinitro-, and hydroxynitrophenyl-substituted 4,7-phenanthrolines were reduced with tin(II) chloride in a mixture of acetic and nitric acids to obtain amino, diamino, and hydroxy derivatives of 4,7-phenanthroline. When heated with aromatic aldehydes, the products form azomethines of the 4,7-phenanthroline series.
Condensation of arylmethylene(6-quinolyl)amines with hydroxy- and nitro-substituted acetophenones was used to synthesize 1,3-diaryl-4,7-phenanthrolines containing hydroxy and nitro groups in the phenyl rings.