Related Experiment Video
Updated: Jan 9, 2026

Heterogeneous Removal of Water-Soluble Ruthenium Olefin Metathesis Catalyst from Aqueous Media Via Host-Guest Interaction
Published on: August 23, 2018
Ruthenium-Catalyzed Electrochemical Ketone Hydrogenation to Secondary Alcohols with High Activity and Selectivity
Xuan Liu1, Cejun Hu2, Na Guo3,4
1Department of Environmental Science and Engineering, School of Energy and Power Engineering, Xi'an Jiaotong University, Xi'an, 710072, China.
None:
Secondary alcohols are indispensable building blocks in the production of fine chemicals, pharmaceuticals, and polymers, yet their conventional synthesis routes are energy and resource intensive. Electrochemical ketone hydrogenation under ambient conditions offers an attractive approach to synthesize secondary alcohols, but this process is often hindered by base-catalyzed self-condensation, hydrogenolysis, and competitive hydrogen evolution reaction (HER). Herein, we demonstrate that Ru nanoparticles supported on commercial carbon black (RuNP/C) can enable efficient, selective, and stable electrochemical hydrogenation of a wide range of structurally diverse ketones to produce corresponding secondary alcohols under ambient conditions. Mechanistic investigations reveal that RuNP/C can simultaneously promote generation of reactive hydrogen species and adsorption of ketone molecules, facilitating rapid transfer of reactive hydrogen species to adsorbed ketone molecules, thereby enabling efficient secondary alcohols formation and suppressing HER. This work opens a green and sustainable pathway for ketone upgrading.
Related Concept Videos
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Reduction of Alkenes: Catalytic Hydrogenation
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
Acid-Catalyzed α-Halogenation of Aldehydes and Ketones
In the first step of the mechanism, the acid protonates the carbonyl oxygen resulting in a resonance-stabilized cation, which subsequently loses an α-hydrogen to form an enol tautomer. The C=C bond in an enol is highly nucleophilic because of the electron-donating nature of the –OH group. Consequently, the double bond attacks an electrophilic halogen to form a...
Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
α-Alkylation of Ketones via Enolate Ions

