Abstract
The reactions of monoethanolamine with 4-nitrophenyl esters of tetracoordinated phosphorus acids in chloroform in the presence of 2-hydroxyethyldimethylpentadecylammonium bromide were studied. The effective rate constants of the reactions are increased by more than two orders of magnitude in the presence of the micelle-forming cationic surfactant. The latter also favors the formation of the product ofO-phosphorylation of monoethanolamine and leads to the appearance of a new ionic form of the 4-nitrophenol-monoethanolamine complex.
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