Castro Enrique A, Cubillos María, Santos José G
Facultad de Química, Pontificia Universidad Católica de Chile, Casilla 306, Santiago 22, Chile.
J Org Chem. 2004 Jul 9;69(14):4802-7. doi: 10.1021/jo049559y.
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
在25.0℃、离子强度为0.2M(KCl)的水中对标题反应进行动力学研究。通过分光光度法跟踪反应,观察到两个连续反应:第一个是相应的硫代氨基甲酸盐(1-(芳氧基硫代羰基)吡啶阳离子)的形成,第二个是它们分解为相应的苯酚、吡啶和COS。在过量胺的情况下得到了准一级速率系数(分别为k(obsd1)和k(obsd2))。在恒定pH下,k(obsd1)对游离吡啶浓度的作图呈线性,斜率(k(N))与pH无关。对于苯基和4-硝基苯基氯硫代甲酸酯的反应,布仑斯惕型作图(log k(N)对吡啶共轭酸的pK(a))呈线性,斜率β分别为0.07和0.11。这些布仑斯惕斜率与在水中相同吡啶的其他逐步反应中发现的斜率一致,在这些反应中,四面体中间体的形成是速率决定步骤。与标题反应的逐步机理相反,相同底物与苯酚的反应是协同的,这意味着在四面体中间体中吡啶基部分被苯氧基取代会使中间体不稳定。第二个反应对应于相应的1-(芳氧基硫代羰基)吡啶阳离子的吡啶催化水解。在恒定pH下,k(obsd2)对游离吡啶浓度的作图呈线性,斜率(k(H))与pH无关。对于苯基和4-硝基苯基衍生物的反应,k(H)的布仑斯惕作图呈线性,斜率β分别为0.19和0.26。这些低值可以用以下事实来解释:随着pK(a)的增加,更好的吡啶催化剂的作用被相应硫代氨基甲酸盐中更差的离去吡啶所补偿。