Shtamburg, V. G.Tsygankov, A. V.Shtamburg, V. V.Anishchenko, A. A.Mazepa, A. V.Kostyanovsky, R. G.2018-06-252018-06-252014Methanolysis of N-acetoxy-N-n-propyloxy-N’,N’-dimethylurea in different conditions / V. G. Shtamburg [et al.] // European Chemical Bulletin. – 2014. – Vol. 3, № 9. – P. 869-872.https://repository.kpi.kharkov.ua/handle/KhPI-Press/36902The methanolysis of N-acetoxy-N-n-propyloxy-N’,N’-dimethylurea in the presence of strong acids at room temperatures or in the boiling methanol yields N,N-dimethoxy-N’,N’-dimethylurea as final product. Primarily the nucleophilic substitution acetoxy group at nitrogen on methoxy group arises. At second stage the transesterification of N,N-dialkoxyamino group of formed N-methoxy-N-n-propyloxy-N’,N’-dimethylurea take place.ennucleophilic substitutionnitrogenN-acyloxy-N-alkoxyureasN,N-dialkoxyureasmethanolysisArticle