Quinazolines. Part XI. Kinetics of methoxy-dehalogenation in 5-, 6-, 7-, and 8-substituted quinazolines in methanol
Abstract
A kinetic study of the displacement of fluorine and chlorine from the benzo-ring of quinazoline by methoxide ions in methanol showed the order of reactivity at the different positions to be 7- > 5- > 6- and 8-, and the fluorosubstituent was displaced more readily than the chloro-substituent. The Arrhenius parameters for these reactions are given.