The hydrodeoxygenation of furfural (FF) over Mo carbides in liquid phase at 200 °C, 30 bar of H₂ for 4 h in 2‐butanol was investigated. Unsupported and SiO₂‐supported Mo carbide with different crystallographic phases (β‐Mo₂C/SiO₂ and α‐MoC/SiO₂), and in the presence of Cu and Ni as promoters were studied. The reactivation treatment under H₂ atmosphere of the passivated Mo carbides was investigated by XAS. The results show that Mo is present in different states of oxidation in the passivated catalysts, with more severe oxidation in the bimetallic systems, in which the original carbides are not restored after reactivation. Finally, the product distribution in the HDO of furfural is modified as a function of catalyst oxidation degree. Using the less oxidized Mo carbide (β‐Mo₂C), a higher yield to 2‐methylfuran is obtained, while C₁₀ condensation products are formed for the more oxidized catalysts.