Catalysis of ester hydrolysis by N-(2-dimethylaminoethyl)acetohydroxamic acid (I)
1975; Elsevier BV; Volume: 4; Issue: 3 Linguagem: Inglês
10.1016/0045-2068(75)90033-4
ISSN1090-2120
AutoresWilliam B. Gruhn, Myron L. Bender,
Tópico(s)Chemical Reactions and Isotopes
ResumoAbstract N-(2-dimethylaminoethyl)acetohydroxamic acid was synthesized. This compound, which incorporates a dimethylamino group as a second functionality into the hydroxamic acid molecule, catalyzes the hydrolysis of p-nitrophenyl acetate faster than acetohydroxamic acid itself does. The function of the dimethylamino group is to labilize the intermediate formed in the reaction, thus assisting deacylation intramolecularly. The dimethylamino group carries out this function by intramolecular general base catalysis. Nucleophilic catalysis is ruled out by the sizable deuterium oxide solvent isotope effect ( k H 2 O k D 2 O = 2.05 ) found. General acid-hydroxide ion catalysis is ruled out by determination of the lack of reaction with azide ion, which does not possess a dissociable proton, with the intermediate in this reaction. The deuterium oxide solvent isotope effect on the azide ion reaction of the intermediate also rules out a general acid-hydroxide ion reaction.
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