A Kinetic Study of the Acid-Catalyzed Hydrolysis of Procainamide * *Rutgers University College of Pharmacy, Newark 4, New Jersey

Author(s):  
Arnold D. Marcus ◽  
Anthony J. Taraszka
1980 ◽  
Vol 45 (7) ◽  
pp. 1959-1963 ◽  
Author(s):  
Dušan Joniak ◽  
Božena Košíková ◽  
Ludmila Kosáková

Methyl 4-O-(3-methoxy-4-hydroxybenzyl) and methyl 4-O-(3,5-dimethoxy-4-hydroxybenzyl)-α-D-glucopyranoside and their 6-O-isomers were prepared as model substances for the ether lignin-saccharide bond by reductive cleavage of corresponding 4,6-O-benzylidene derivatives. Kinetic study of acid-catalyzed hydrolysis of the compounds prepared was carried out by spectrophotometric determination of the benzyl alcoholic groups set free, after their reaction with quinonemonochloroimide, and it showed the low stability of the p-hydroxybenzyl ether bond.


1968 ◽  
Vol 33 (8) ◽  
pp. 3174-3178 ◽  
Author(s):  
Jerome P. Horwitz ◽  
Chittur V. Easwaran ◽  
Leon S. Kowalczyk

2012 ◽  
Vol 40 (6) ◽  
pp. 389-396
Author(s):  
Young-Jun Seo ◽  
Hong-Joo Lee ◽  
Jae-Won Lee

2007 ◽  
Vol 46 (6) ◽  
pp. 1696-1708 ◽  
Author(s):  
B. Girisuta ◽  
L. P. B. M. Janssen ◽  
H. J. Heeres

1953 ◽  
Vol 31 (4) ◽  
pp. 361-376 ◽  
Author(s):  
A. V. Willi ◽  
R. E. Robertson

The rates of the acid catalyzed hydrolysis of a series of para substituted benzalanilines have been studied in 50/50 methanol–water in the presence of acetate buffers. Special and general acid catalysis were observed. The effect of para substituents on the rate is different for the charged and uncharged catalyst, and Hammett's relation cannot be applied. Similarly the effect of substituents on the Arrhenius constants for the two cases is different. The para dimethylamino derivative provides an interesting special case. For low buffer concentrations and in unbuffered solutions certain deviations were observed which show that the dependence of the rate on the catalyst concentration is more complicated than the equation[Formula: see text]


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