E-Selective Manganese-Catalyzed Semihydrogenation of Alkynes with H2 Directly Employed or In Situ-Generated

Selective semihydrogenation of alkynes with the Mn(I) alkyl catalyst fac-[Mn(dippe)(CO)(3)(CH2CH2CH3)] (dippe = 1,2-bis(di-iso-propylphosphino)ethane) as a precatalyst is described. The required hydrogen gas is either directly employed or in situ-generated upon alcoholysis of KBH4 with methanol. A series of aryl-aryl, aryl-alkyl, alkyl-alkyl, and terminal alkynes was readily hydrogenated to yield E-alkenes in good to excellent isolated yields. The reaction proceeds at 60 degrees C for directly employed hydrogen or at 60-90 degrees C with in situ-generated hydrogen and catalyst loadings of 0.5-2 mol %. The implemented protocol tolerates a variety of electron-donating and electron-withdrawing functional groups, including halides, phenols, nitriles, unprotected amines, and heterocycles. The reaction can be upscaled to the gram scale. Mechanistic investigations, including deuterium-labeling studies and density functional theory (DFT) calculations, were undertaken to provide a reasonable reaction mechanism, showing that initially formed Z-isomer undergoes fast isomerization to afford the thermodynamically more stable E-isomer.

Automated summary

This study describes the selective semihydrogenation of alkynes using a Mn(I) alkyl catalyst, leading to good to excellent yields of E-alkenes. Mechanistic investigations reveal that the initially formed Z-isomer undergoes fast isomerization to the thermodynamically more stable E-isomer.