Selective, efficient nanoporous catalysts for nitroaldol condensation: Co-placement of multiple site-isolated functional groups on mesoporous materials

We recently reported the synthesis of efficient multifunctional catalysts for the Henry reaction by grafting aminopropyl groups on mesoporous silica with polar, protic solvents such as ethanol [K.K. Sharma, T. Asefa, Angew. Chem. Int. Ed. 46 (2007) 2879-2882]. Here we describe that the grafting of aminopropyl groups with secondary organic functional groups in polar solvents results in selective efficient nanoporous catalysts for hydrophilic or hydrophobic reactants in the Henry reaction. In the synthesis, a mixture of ammorganosilanes and secondary organosilanes containing ureidopropyl, 3-mercaptopropyl, or methyl groups was reacted with the silanol groups of mesoporous silica in isopropanol. While the 3-aminopropyl groups introduced solid-base catalytic sites, the secondary functional groups and the residual ungrafted silanols on the materials modified the catalyst's surface to either hydrophilic or hydrophobic. More importantly, by grafting the organosilanes in isopropanol, site-isolated multifunctional groups and high surface area mesoporous solid-base catalysts resulted, which afforded not only selectivity for hydrophilic or hydrophobic reactants but also high percentage conversion (similar to 100%) of various p-substituted benzaldehydes within 15-30 min of the Henry reaction. Furthermore, the time to achieve the maximum selectivity for hydrophilic or hydrophobic reactants in mixtures of p-substituted benzalclehydes was obtained. These results are significant compared to examples of previously reported selective catalysts, which showed selectivity only for hydrophobic reactants with a maximum selectivity of 2.6:1.0, and a highest conversion of 50% in 24 h [J. Huh, et al., J. Am. Chem. Soc. 126 (2004) 1010-1011]. Our synthetic approach can be extended to other reactants and reactions by judiciously choosing and grafting multiple organic groups in polar, protic solvents. (C) 2008 Elsevier B.V. All rights reserved.