Abstract
This communication proposes a preliminary simplified kinetic model for the hydrogenation of 1-phenyl-1,2-propanedione that can render up to eight compounds, involving regioselectivity and enantioselectivity. The catalytic system comprises two functionalities; the heterogeneous catalyst (Ir/TiO(2)) plays the role for the hydrogenation, whereas the adsorption/binding to the active site is played by a chiral molecule (cinchonidine), added to the reaction mixture. The reaction occurs at room temperature and total pressure of 40 bar. The product distribution shows competitive parallel and series pathways with up to 12 possible reactions. Despite the complexity of both reaction and catalyst system, a simplified kinetic model was able to predict the concentrations profiles. The model assumes the reactions to be apparent first order in the concentrations of reactant and intermediate products, while the kinetic constants include all other effects (partial pressure of hydrogen, solvent and catalyst effects, and the concentration of the chiral additive). The concentration profiles were well-modeled with low residual values. The errors in the kinetic constants (k-values) were small for all relevant parameters of the main reaction pathways. Two k-values are nil, which is the lower bound imposed in the model, suggesting that these reaction pathways are likely negligible. The positive outcome from this simplified model suggests that the process can be formally treated as a first-order irreversible homogeneous catalyzed reaction, despite a heterogeneous catalyst was employed (with a modifier). Despite the promising results, the model must be extended for a more general applicability, or conditions where it is applicable.