Substituent effects on thermal rearrangement of 3- (substituted phenyl)-4-(p-tolyl)-1,2,4-oxadiazole-5(4H)-thiones
作者:Hikmet Agirbas、Alev Toker
DOI:10.1002/1099-1395(200101)14:1<58::aid-poc337>3.0.co;2-o
日期:2001.1
The kinetics of the rearrangement of 3-(substituted phenyl)-4-(p-tolyl) 1,2,4-oxadiazole-5(4H)-thiones in solution were determined in the temperature range 160-200 C-degrees. From the correlation of logk against sigma, it was found that for m-Me, p-Cl and p-CN, the compounds rearrange with the homolytic cleavage of the N-O bond, whereas for p-Me, H and m-NO2, the rearrangement occurs with the heterolytic cleavage of the N-O bond. In comparison with the uncatalysed rearrangement, Cu catalysis greatly increased the rate of the rearrangement of 3-(m-chlorophenyl)-4-(p-tolyl)-1,2,4-oxadiazole-5(4H)-thione at 166 degreesC. Copyright (C) 2000 John Wiley & Sons, Ltd.