Related Experiment Video
Updated: Jan 15, 2026

A Microwave-Assisted Direct Heteroarylation of Ketones Using Transition Metal Catalysis
Published on: February 16, 2020
Rapid and Practical Transfer Hydrogenation for Cleavage of N‑Cbz Protected Amines Using a Supported Palladium
Paige A Horsley1, J Craig Ruble1, Nicholas P R Onuska1
1Lilly Small Molecule Discovery, Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, Indiana 46285, United States.
Abstract:
Hydrogenation reactions are commonly employed to reduce organic functional groups, but traditional approaches often rely on hazardous compressed gases and pyrophoric catalysts. Motivated by the need for safer and more practical alternatives, we developed a broadly applicable protocol for Cbz group removal that avoids both flammable Pd/C and hydrogen cylinders. Instead, we utilize SiliaCatPd(0)a commercially available, sol-gel supported palladiumwhich has demonstrated effectiveness in debenzylation processes. The unique sol-gel matrix of this catalyst minimizes metal leaching and mitigates the risks associated with pyrophoric palladium sources. Leveraging these advantages, our method offers a safer and more convenient route for hydrogenation in everyday laboratory practice. Specifically, we present a transfer hydrogenation system using this supported palladium catalyst for the selective deprotection of Cbz-protected amines, designed to streamline medicinal chemistry workflows with rapid setup and execution in a microwave reactor.
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 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.
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...
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation reactions,...
Radical Anti-Markovnikov Addition to Alkenes: Overview
Preparation of Amines: Reduction of Amides and Nitriles
Amides can be reduced to primary, secondary, and tertiary amines using catalytic hydrogenation, active metals like Fe,...

