Abstract The cleavage of CO bonds in lignin model compounds without hydrogen was developed using the commercially available Pd/C. Hydrogen donor solvents are helpful for this reaction through transfer hydrogenation, but not necessary. A redox neutral process that utilizes the internal hydrogen source for the cleavage is also possible. An initial mechanistic study indicates that the β‐benzylic‐H atom in the substrate plays a critical role and that the present system undergoes a process different from previous reports.