Scientific journal
Название журнала на английском
ISSN 2500-0802
ПИ №ФС77-61154

ABOUT THE TRANSFORMATIONS PHENOXYPROPIONIC UNDER THE REACTION CONDITIONS OF NITROSATION

Gazzaeva R.A. 1 Koblova L.B. 1 Khabaeva Z.G. 1 Gagloeva M.T. 1
1 North-Osetian State University
When reacting phenoxycyclopropane derivatives and phenoxyallyl with nitrous acid formed in situ, nitrosation takes place either in the aromatic nucleus, or in the small ring. The interaction of the halogenated cyclopropane derivatives phenoxy nitrosation reaction conditions and the competing influence of the small loop and phenoxy substituents in derivatives of the example cyclopropyl-methylphenyl ether and 2-cyclopropylphenoxyallyl. It has been established that the interaction of the test compounds does not proceed regioselectively. Synthesized compounds by reaction with nitrous acid formed in situ, advantageous subjected disclosure small loop to form heterocyclic structures expected. The resulting compounds were analyzed for growth promoting activity. It is shown that the optimal concentration limits, with pronounced growth promoting activity constitute 0.01-0.001 mas.%.