Alkylation of 3-Trifluoromethyl-1,2-dihydroquinoxalin-2-one


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详细

O and N centers of 3-trifluoromethyl-1,2-dihydroquinoxalin-2-one anion shows in reactions with haloalkanes an ambident nucleophilic character. The chemoselectivity of the reaction depends on the alkylating agent: the methylation of 3-trifluoromethyl-1,2-dihydroquinoxalin-2-one in acetonitrile in the presence of K2CO3 yields only an N-methyl isomer whereas under the same conditions in the reaction with (4-bromobutyl)-acetate О- and N-alkylations are competing.

作者简介

A. Ivanova

Postovskii Institute of Organic Synthesis, Ural branch

Email: saloutin@ios.uran.ru
俄罗斯联邦, ul. S. Kovalevskoi/Akademicheskaya 22/20, Yekaterinburg, 620990

Ya. Burgart

Postovskii Institute of Organic Synthesis, Ural branch

Email: saloutin@ios.uran.ru
俄罗斯联邦, ul. S. Kovalevskoi/Akademicheskaya 22/20, Yekaterinburg, 620990

M. Pervova

Postovskii Institute of Organic Synthesis, Ural branch

Email: saloutin@ios.uran.ru
俄罗斯联邦, ul. S. Kovalevskoi/Akademicheskaya 22/20, Yekaterinburg, 620990

S. Borisevich

Ufa Institute of Chemistry

Email: saloutin@ios.uran.ru
俄罗斯联邦, pr. Oktyabrya 71, Ufa, Bashkortostan, 450054

S. Khursan

Ufa Institute of Chemistry

Email: saloutin@ios.uran.ru
俄罗斯联邦, pr. Oktyabrya 71, Ufa, Bashkortostan, 450054

V. Saloutin

Postovskii Institute of Organic Synthesis, Ural branch

编辑信件的主要联系方式.
Email: saloutin@ios.uran.ru
俄罗斯联邦, ul. S. Kovalevskoi/Akademicheskaya 22/20, Yekaterinburg, 620990

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