An effective and applicable deuteration method for alkyl-substituted aromatic compounds using a heterogeneous Pd/C and Pt/C mixed catalyst in deuterium oxide in the presence of a small amount of hydrogen gas was developed. Mixing a heterogeneous palladium and platinum catalyst provides an interesting synergistic effect in the H-D exchange reaction and leads to full H-D exchange results even on sterically hindered sites, which indicated only low-deuterium efficiencies when either Pd/C or Pt/C were used independently as a catalyst. We investigated the synergistic effect using a variety of substrates and proved the broad generality of the heterogeneous Pd-Pt-D2O-H2 system in the H-D exchange reaction. Furthermore, this system could be applied to a multigram scale synthesis of useful deuterium-labeled compounds, such as deuterium-labeled bis-aniline derivatives as raw materials for polyimides, aryl iodides as synthetic building blocks, and biologically active compounds.
An effective and applicable deuteration method for aromatic rings using Pt/C–D2O–H2 system was established. Especially, phenol was fully deuterated even at room temperature, and other electron-rich aromatic nuclei were efficiently deuterated under mild conditions. The scope and limitations of the presence method and its application to the synthesis of deuterium-labeled biologically active compounds and deuterium-labeled building blocks for practical multi-gram scale syntheses are reported.