Kinetics of the hydrogenation of alkyl levulinates to γ-valerolactone over Ru/C were investigated. γ-Valerolactone with 85% selectivity was produced from methyl levulinate after 5 h. Substrates with shorter alkyl residue show higher selectivity toward γ-valerolactone. Kinetic modeling indicates lactonization as the rate determining step. Activation energies of hydrogenation and lactonization increaseas methyl levulinate<ethyl levulinate<butyl levulinate.