Solvent Effects on a Diels−Alder Reaction Involving a Cationic Diene:  Consequences of the Absence of Hydrogen-Bond Interactions for Accelerations in Aqueous Media

In order to study the influence of hydrogen-bond interactions on the accelerations of Diels−Alder reactions in water and highly aqueous mixed solvent systems, second-order rate constants for the Diels−Alder reaction of acridizinium bromide (1a) with cyclopentadiene (CP) have been measured in aqueous media and organic solvents. Only modest rate accelerations were found in water-rich media. This is attributed to the absence of hydrogen-bonding groups in the reactants. Comparison with cycloadditions of CP with 9-carbomethoxyacridizinium bromide (1b), acrylonitrile (3), and methyl vinyl ketone (4), which do contain hydrogen-bond acceptors, reveals substantially larger aqueous accelerations. These results demonstrate that hydrogen bonding is a major factor in aqueous accelerations. Also rate constants for the cycloaddition of CP to 1a in surfactant solutions were determined. Micellar catalysis is observed in SDS solutions, due to binding of both the diene and the dienophile to the anionic micellar surface.