Sustainable amidation through acceptorless dehydrogenative coupling by pincer-type catalysts: recent advances

The amide functional group is ubiquitous in living organisms, and is of particular importance in bioactive compounds and pharmaceuticals. Because of the prevalence and significance of the amide bond, considerable efforts have been invested throughout the years in developing new synthetic methodologies for its formation. Nevertheless, amide synthesis still largely relies on variants of the traditional condensation of carboxylic acids and amines, mediated by stoichiometric coupling reagents. This poses a sustainability challenge, since such reactions suffer from unfavorable atom and step economies, involve harmful chemicals and produce chemical waste. Hence, establishing sustainable approaches to amide synthesis is of great importance. Over the last two decades, we have developed homogeneous catalytic reactions for sustainable synthetic transformations, primarily based on transition metal complexes of pincer ligands. A considerable portion of these efforts has been devoted to acceptorless dehydrogenative coupling, including that of alcohols and amines through ruthenium-catalyzed reactions. These latter processes generate amides without resorting to coupling reagents and typically produce no waste, with their only byproduct being H-2 gas, which is itself a valuable resource. In the present review, we chronicle our progress in this area of research since 2014. This includes the use of water and ammonia as amidation reagents, expanding the scope of amidation substrates and target amides, achieving milder reaction conditions, development of amidation-based liquid organic hydrogen carrier systems, and introduction of manganese-based catalysts.

Automated summary

The amide functional group is widely distributed in living organisms and is particularly important in bioactive compounds and pharmaceuticals. However, the current method for amide synthesis relies heavily on traditional condensation reactions, which pose sustainability challenges. Therefore, developing sustainable approaches to amide synthesis is essential. Over the past two decades, homogeneous catalytic reactions, particularly ruthenium-catalyzed acceptorless dehydrogenative coupling, have been developed to achieve amide synthesis without coupling reagents and waste generation, with H-2 gas being the only byproduct.