Abstract: | The condensation of hydrochlorides of ethyl iminoesters of 4-hydroxy-3,5-di-tert-butylbenzoic and -(4-hydroxy-3,5-di-tert-butylphenyl) propionic acids with monoethanolamine, o-aminophenol, and o-phenylenediamine was studied. As a result, 2-oxazolines, benzoxazoles, and benzimidazoles containing sterically hindered phenol residues in the 2-position were synthesized.For Communication 34, see [1].Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 889–892, July, 1984. |