The transfer hydrogenation of organic compounds is a much safer and more environmentally benign process than reduction reactions involving molecular hydrogen, metal hydrides, or dissolving metals. In transfer hydrogenation, 2-propanol is often preferred as the source of hydrogen because it is cheap, easy to remove, and environmentally friendly. This class of transformation has been mostly pursued through the use of expensive noble metals, such as Ru, Pd, and so forth; research involving cheaper catalytically active metals has been relatively neglected. On the other hand, alcohols have recently emerged as desirable alkylating agents, a useful alternative to organic halides, in reactions of hydrogen autotransfer, also known as the "borrowing of hydrogen" methodology. For instance, the α-alkylation of ketones with alcohols is an atom-efficient process that produces water as the only byproduct in the presence of a noble metal catalyst. Hydrogen autotransfer is also successful in the synthesis of amines through a reductive aza-Wittig reaction, which involves an iminophosphorane and primary alcohol under iridium catalysis. The in situ oxidation-Wittig olefination of primary alcohols with stabilized phosphorus ylides is a commonly practiced method in organic synthesis that precludes the necessity of handling aldehydes. These reactions are normally performed in one pot but sequentially; thus the course of the alcohol oxidation needs monitoring before the ylide addition. In this Account, we describe the development of our discovery that nickel(0), in the form of nanoparticles, can replace the more expensive noble metals in both transfer hydrogenation and hydrogen autotransfer reactions. These nanoparticles were found to catalyze the transfer hydrogenation of olefins and carbonyl compounds, as well as the reductive amination of aldehydes, with 2-propanol as the hydrogen donor. All reactions proceeded in the absence of base, and the catalyst could be easily and successfully reutilized in the case of the carbonyl compounds. The catalyst was fully characterized, and the reaction mechanism, kinetics, and heterogeneous nature of the process were established through a variety of experiments. Moreover, the nickel nanoparticles enabled the activation of primary alcohols for the α-alkylation of ketones and reductive aza-Wittig reaction, with the latter leading to secondary amines. For the first time, these two reactions were achieved with a catalyst that was not one of the noble metals. We also observed that nickel nanoparticles can activate alcohols in the presence of phosphorus ylides. In this case, although the autotransfer of hydrogen failed, the reaction could be used as a key tool to construct carbon-carbon double bonds. In this respect, we describe the one-pot synthesis of stilbenes from alcohols through a Wittig-type olefination reaction promoted by nickel nanoparticles. We report a wide range of polymethoxylated and polyhydroxylated stilbenes, including the naturally occurring polyphenol resveratrol. The utility of the nickel nanoparticles was exceptional in all of the aforementioned reactions when compared with other forms of nickel, including Raney nickel.
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Apr 21, 2011
Chen Liu + 3
Open Access