Selective synthesis of novel cyclic phenylazomethine trimers

Novel cyclic phenylazomethine trimers (CPAs) were synthesized in a one-step dehydration of the 4-aminobenzophenone derivatives in the presence of TiCl4 or p-toluenesulfonic acid (PTS). The CPAs were isolated in over 90% yield under nondilute conditions. When using TiCl4 as the dehydration agent, the induction of bulky substituents at the alpha-position of the substrate enhanced the yields of the CPAs. On the other hand, PTS served as an effective catalyst for the synthesis of the phenyl-substituted CPA. This different reactivity between TiCl4 and PTS depends on the dehydration mechanism being dominated by a kinetic process or thermodynamic one. The obtained CPAs were confirmed by NMR, UV-vis spectra, and MM2 calculation to have only a Z conformation and a nonconjugated structure compared to the Linear oligophenylazomethines (OPAs) and the aniline-capped OPAs (OPA's).