Literature DB >> 15230606

Kinetics and mechanisms of the pyridinolysis of phenyl and 4-nitrophenyl chlorothionoformates. Formation and hydrolysis of 1-(aryloxythiocarbonyl)pyridinium cations.

Enrique A Castro1, María Cubillos, José G Santos.   

Abstract

The title reactions are subjected to a kinetic study in water, at 25.0 degrees C, and an ionic strength of 0.2 M (KCl). By following the reactions spectrophotometrically two consecutive reactions are observed: the first is formation of the corresponding thionocarbamates (1-(aryloxythiocarbonyl)pyridinium cations) and the second is their decomposition to the corresponding phenol and pyridine, and COS. Pseudo-first-order rate coefficients (k(obsd1) and k(obsd2), respectively) are found under excess amine. Plots of k(obsd1) vs free pyridine concentration at constant pH are linear, with the slope (k(N)) independent of pH. The Brønsted-type plots (log k(N) vs pK(a) of the conjugate acids of the pyridines) are linear with slopes beta = 0.07 and 0.11 for the reactions of phenyl and 4-nitrophenyl chlorothionoformates, respectively. These Brønsted slopes are in agreement with those found in other stepwise reactions of the same pyridines in water, where the formation of a tetrahedral intermediate is the rate-determining step. In contrast to the stepwise mechanism of the title reactions that for the reactions of the same substrates with phenols is concerted, which means that substitution of a pyridino moiety in a tetrahedral intermediate by a phenoxy group destabilizes the intermediate. The second reaction corresponds to the pyridine-catalyzed hydrolysis of the corresponding 1-(aryloxythiocarbonyl)pyridinium cation. Plots of k(obsd2) vs free pyridine concentration at constant pH are linear, with the slope (k(H)) independent of pH. The Brønsted plots for k(H) are linear with slopes beta = 0.19 and 0.26 for the reactions of the phenyl and 4-nitrophenyl derivatives, respectively. These low values are explained by the fact that as pK(a) increases the effect of a better pyridine catalyst is compensated by a worse leaving pyridine from the corresponding thionocarbamate

Entities:  

Year:  2004        PMID: 15230606     DOI: 10.1021/jo049559y

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  7 in total

1.  Understanding Solvent Effects in the Solvolyses of 4-Fluorophenyl Chlorothionoformate.

Authors:  Mj D'Souza; Sm Hailey; Bp Mahon; Dn Kevill
Journal:  Chem Sci J       Date:  2011-06-27

2.  Syntheses of Salmonella Paratyphi A Associated Oligosaccharide Antigens and Development towards Anti-Paratyphoid Fever Vaccines.

Authors:  Debashis Dhara; Scott M Baliban; Chang-Xin Huo; Zahra Rashidijahanabad; Khandra T Sears; Setare Tahmasebi Nick; Anup Kumar Misra; Sharon M Tennant; Xuefei Huang
Journal:  Chemistry       Date:  2020-10-22       Impact factor: 5.236

3.  Use of empirical correlations to determine solvent effects in the solvolysis of S-methyl chlorothioformate.

Authors:  Malcolm J D'Souza; Stefan M Hailey; Dennis N Kevill
Journal:  Int J Mol Sci       Date:  2010-05-25       Impact factor: 5.923

4.  Analysis of the nucleophilic solvation effects in isopropyl chlorothioformate solvolysis.

Authors:  Malcolm J D'Souza; Brian P Mahon; Dennis N Kevill
Journal:  Int J Mol Sci       Date:  2010-06-29       Impact factor: 5.923

5.  Evaluation of Electronic Effects in the Solvolyses of p-Methylphenyl and p-Chlorophenyl Chlorothionoformate Esters.

Authors:  Malcolm J D'Souza; Olivia N Hampton; Brett M Sansbury; Dennis N Kevill
Journal:  J Chem       Date:  2013

6.  Kinetic evaluation of the solvolysis of isobutyl chloro- and chlorothioformate esters.

Authors:  Malcolm J D'Souza; Matthew J McAneny; Dennis N Kevill; Jin Burm Kyong; Song Hee Choi
Journal:  Beilstein J Org Chem       Date:  2011-04-29       Impact factor: 2.883

7.  Influence of sulfur for oxygen substitution in the solvolytic reactions of chloroformate esters and related compounds.

Authors:  Malcolm J D'Souza; Dennis N Kevill
Journal:  Int J Mol Sci       Date:  2014-10-10       Impact factor: 5.923

  7 in total

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