Collect. Czech. Chem. Commun.
1987, 52, 140-155
https://doi.org/10.1135/cccc19870140
Kinetics and mechanism of base-catalyzed cyclization of substituted amides and nitriles of hydantoic acid
Vladimír Macháčeka, Gabriela Svobodováb and Vojeslav Štěrbaa
a Department of Organic Chemistry, Institute of Chemical Technology, 532 10 Pardubice
b Research Institute of Organic Syntheses, 532 18 Pardubice-Rybitví
Abstract
Rates of base-catalyzed cyclizations of 8 substituted derivatives of hydantoic acid amide type R3-NH(5)-CO(4)-NR2(3)-CH2(2)-CO(1)-NHR1 and 9 nitriles type R3-NH(5)-CO(4)-NR2(3)-CHR1(2)-CN have been measured in aqueous and methanolic media. The cyclization of the amides in aqueous medium is also accompanied by hydrolysis of the hydantoins formed. In some cases the hydrolysis rate constant is greater than the corresponding cyclization reaction rate constant. With the least reactive amides, the cyclization is also accompanied by hydrolysis of the amide group. The rate of the cyclization reactions in water is higher than that in methanol (at the same concentration of the lyate ions) by the factor of 10-100. Substitution of hydrogen at 3 and 5 positions by methyl or phenyl groups causes an acceleration of the cyclization reaction, whereas a substitution in the amide group causes a considerable retardation. The greatest acceleration of the cyclization (by as much as 4 orders) is caused by introduction of phenyl group to the N(5) position, which is due to a substantial increase of concentration of the reactive anion.
