Improved Halogenation of Methyl Aromatics and Methyl Heteroaromatics: Unexpected Reactivity of Tetrahalogeno-diphenylglycolurils

Abstract : 1,3,4,6-Tetrachloro (TCDGU) and 1,3,4,6-tetrabromo-3α,6α-diphenylglycolurils smooth halogen oxidizers have been exploited in a new direction as reagents for free radical substitution toward some N-halosuccinimide nonreactive bis-heterocycles. An unexpected selectivity and reactivity were observed with methyl benzenes, methyl heterocycles, and methyl-bis-heterocycles of interest. A chemometric study has been performed to optimize five independent factors of the chlorination reaction with TCDGU. The predictive model was established either for the halogenation conversion and the ratio of monochlorination.
Type de document :
Article dans une revue
Heteroatom Chemistry, Wiley, 2015, 27 (3), pp.173 - 183. 〈10.1002/hc.21314〉
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https://hal.univ-lorraine.fr/hal-01496159
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Soumis le : lundi 27 mars 2017 - 11:32:27
Dernière modification le : mardi 16 janvier 2018 - 10:24:44

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Florian Moretti, Guillaume Poisson, Alain Marsura. Improved Halogenation of Methyl Aromatics and Methyl Heteroaromatics: Unexpected Reactivity of Tetrahalogeno-diphenylglycolurils. Heteroatom Chemistry, Wiley, 2015, 27 (3), pp.173 - 183. 〈10.1002/hc.21314〉. 〈hal-01496159〉

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