Abstract
The mechanism of hydrolysis of esters of triazine substitutes was studied. It was shown that hydrolysis of l-menthyl esters in both alkaline and acid media at 80–120° C takes place with cleavage of the bond between the oxygen and carbon of triazine. The bond between the oxygen and carbon of alcohol is broken at 180–200° C in acid medium. The kinetics of alkaline hydrolysis of triazine esters was studied, and it was established that the stability of the latter increases in relation to the influence of the substitute in triazine in the order: C6H5 < NHC6H5 < NHC2H5 < N(C2H5)2. A number of new C-substitutes of triazine was synthesized.
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We thank Prof. A. I. Korolev for the proposal, and the attention he gave to this work.
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Mur, V.I., Bedina, Z.A. Hydrolysis of esters of certain substitutes of 1,3,5-triazine. Chem Heterocycl Compd 4, 814–816 (1968). https://doi.org/10.1007/BF00486972
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DOI: https://doi.org/10.1007/BF00486972