Abstract

We report a room-temperature protocol for the hydrogenation of various amides to produce amines and alcohols. Compared with most previous reports for this transformation, which use high temperatures (typically, 100–200 °C) and H2 pressures (10–100 bar), this system proceeds under extremely mild conditions (RT, 5–10 bar of H2). The hydrogenation is catalyzed by well-defined ruthenium-PNNH pincer complexes (0.5 mol %) with potential dual modes of metal–ligand cooperation. An unusual Ru-amidate complex was formed and crystallographically characterized. Mechanistic investigations indicate that the room-temperature hydrogenation proceeds predominantly via the Ru–N amido/amine metal–ligand cooperation.

Highlights

  • We report a room-temperature protocol for the hydrogenation of various amides to produce amines and alcohols

  • Amide hydrogenation can proceed either via C−N bond cleavage or by C−O bond cleavage (Scheme 1).5a,b We are interested in the C−N bond cleavage pathway, which is challenging because of the water losing tendency of the hemiaminal intermediate to form imine

  • Hydrogenation and dehydrogenative formation of the amide bond has been instrumental in the recent development of promising liquid organic hydrogen carrier (LOHC) systems based on alcohols and amines.[7]

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Summary

Ru-2 RT 68 THF

Temperature amide hydrogenation to amines and alcohols catalyzed by the Ru-PNNH complexes at low catalyst loading (0.5 mol %) under low H2 pressures (5−10 bar). Changing the N-substitution of the catalyst from t-Bu to benzyl group (Ru-2), the catalytic activity increased even further, and complete conversion of the amide to the amine and alcohol was observed after 20 h (entry 2). It is likely that the acidic nature of the N-H proton of PNNH ligand assists in lowering the energy requirement of this rate-determining step, allowing the hydrogenation to proceed even at RT via the amido pathway This can explain the higher catalytic activity of Ru-2 compared with Ru1, where the Bn substitution of the N donor atom makes the ligand N-H of Ru-2 less basic as compared with Ru-1 with t-Bu group in the N atom.

■ ACKNOWLEDGMENTS
■ REFERENCES

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