Kinetics and mechanism of large rate enhancement in the Alkaline Hydrolysis of N '-Morpholino-N-(2'-Methoxyphenyl)Phthalamide

Ariffin, A. and Khan, M.N. and Sim, Y.L. (2008) Kinetics and mechanism of large rate enhancement in the Alkaline Hydrolysis of N '-Morpholino-N-(2'-Methoxyphenyl)Phthalamide. Journal of Organic Chemistry, 73 (10). pp. 3730-3737. ISSN 0022-3263

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Official URL: http://pubs.acs.org/doi/pdfplus/10.1021/jo702695k

Abstract

The apparent second-order rate constant (k(OH)) for hydroxide-ion-catalyzed conversion of 1 to N-(2'-methoxyphenyl)phthalamate (4) is similar to 10(3)-fold larger than k(OH) for alkaline hydrolysis of N-morpholinobenzamide (2). These results are explained in terms of the reaction scheme 1 -> 3 -> 4 where 3 represents N-(2'-methoxyphenyl)phthalimide and the values of k(2obs)/k(1obs) Vary from 6.0 x 10(2) to 17 x 10(2) within [NaOH] range of 5.0 x 10(-3) to 2.0 M. Pseudo-first-order rate constants (k(obs)) for alkaline hydrolysis of 1 decrease from 21.7 x 10(-3) to 15.6 x 10(-3) s(-1) with an increase in ionic strength (by NaCl) from 0.5 to 2.5 M at 0.5 M NaOH and 35 degrees C. The values of k(obs), obtained for alkaline hydrolysis of 2 within [NaOH] range 1.0 x 10(-2) to 2.0 M at 35 degrees C, follow the relationship k(obs) = k(OH)[HO(-)] + k(OH)'[HO(-)](2) with least-squares calculated values of k(OH) and k(OH)' as (6.38 +/- 0.15) x 10(-5) and (4.59 +/- 0.09) x 10(-5) M(-2) s(-1), respectively. A few kinetic runs for aqueous cleavage of 1, N'-morpholino-N-(2'-methoxyphenyl)-5-nitrophthalamide (5) and N'-morpholino-N-(2'-methoxyphenyt)-4-nitrophthalamide (6) at 35 degrees C and 0.05 M NaOH as well as 0.05 M NaOD reveal the solvent deuterium kinetic isotope effect (= k(obs)(H2O)/k(obs)(D2O)) as 1.6 for 1, 1.9 for 5, and 1.8 for 6. Product characterization study on the cleavage of 5, 6, and N-(2'-methoxyphenyl)-4-nitrophthalimide (7) at 0.5 M NaOD in D(2)O solvent shows the imide-intermediate mechanism as the exclusive mechanism.

Item Type: Article
Additional Information: Department of Chemistry, Faculty of Science Building, University of Malaya, 50603 Kuala Lumpur, MALAYSIA
Uncontrolled Keywords: Deuterium; Hydrolysis; Kinetics; Magnetic Resonance Spectroscopy/methods; Molecular Structure; Morpholines/*chemistry; Phthalic Acids/*chemistry; Sodium Hydroxide/*chemistry
Subjects: Q Science > QD Chemistry
Divisions: Faculty of Science > Dept of Chemistry
Depositing User: Miss Malisa Diana
Date Deposited: 03 Jul 2013 06:56
Last Modified: 03 Jul 2013 06:56
URI: http://eprints.um.edu.my/id/eprint/8067

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