2023
DOI: 10.1002/slct.202300346
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Ruthenium(III) Chloride as an Efficient Catalyst for the Selective Oxidation of Fatty Alcohols to Aldehydes

Abstract: The oxidation of a series of fatty alcohols to yield the corresponding aldehydes is performed using RuCl3 ⋅ (H2O)x as a homogeneous catalyst and inexpensive trimethylamine N‐oxide (TMAO) as the oxygen source. The reaction conditions were optimized for both high conversion and high selectivity.

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Cited by 2 publications
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“…Ruthenium-based catalysts are among the most active and effective metal-based catalysts in this field, catalyzing this dehydrogenative condensation reaction either with an oxidant (typically, O 2 or air) or even in the absence of any oxidants under an inert atmosphere. While the latter could largely avoid overoxidation of alcohols to carboxylic acids, it might also be faced with a significant decrease in reaction selectivity caused by the formation of amine byproducts as a result of the reaction of imine products with the hydride species generated during the dehydrogenation process. , Moreover, some of the catalytic systems presented for the coupling of alcohols with amines under inert conditions have drawbacks such as using large amounts of poorly accessible, expensive, complex, and yet nonrecyclable homogeneous catalysts, using additives, requiring high reaction temperatures, and needing to conduct the reactions under an Ar/N 2 atmosphere. Therefore, it seems that the aerobic oxidative coupling of alcohols and amines, especially by employing heterogeneous and recoverable catalytic systems, is still an active and preferable approach to the synthesis of imines. However, while the utilization of various Ru catalysts, either in the form of homogeneous or heterogeneous catalytic systems, has been extensively established in the aerobic oxidation of alcohols and/or amines, the use of Ru-based catalytic systems in the one-pot tandem synthesis of imines through the selective oxidative coupling of alcohols and amines is a multifaceted and relatively less explored process.…”
Section: Introductionmentioning
confidence: 99%
“…Ruthenium-based catalysts are among the most active and effective metal-based catalysts in this field, catalyzing this dehydrogenative condensation reaction either with an oxidant (typically, O 2 or air) or even in the absence of any oxidants under an inert atmosphere. While the latter could largely avoid overoxidation of alcohols to carboxylic acids, it might also be faced with a significant decrease in reaction selectivity caused by the formation of amine byproducts as a result of the reaction of imine products with the hydride species generated during the dehydrogenation process. , Moreover, some of the catalytic systems presented for the coupling of alcohols with amines under inert conditions have drawbacks such as using large amounts of poorly accessible, expensive, complex, and yet nonrecyclable homogeneous catalysts, using additives, requiring high reaction temperatures, and needing to conduct the reactions under an Ar/N 2 atmosphere. Therefore, it seems that the aerobic oxidative coupling of alcohols and amines, especially by employing heterogeneous and recoverable catalytic systems, is still an active and preferable approach to the synthesis of imines. However, while the utilization of various Ru catalysts, either in the form of homogeneous or heterogeneous catalytic systems, has been extensively established in the aerobic oxidation of alcohols and/or amines, the use of Ru-based catalytic systems in the one-pot tandem synthesis of imines through the selective oxidative coupling of alcohols and amines is a multifaceted and relatively less explored process.…”
Section: Introductionmentioning
confidence: 99%