Abstract
Nucleophilic substitution reactions of trichloromethyl groups in 2-alkyl-4,6-bis-(trichloromethyl)-sym-triazines by alkoxy radicals were studied. It was shown that in the presence of sodium alcoholates, two CCl3 groups are replaced, and the corresponding 2,4-dialkoxy-6-alkyl-sym-triazines are formed. The products of partial replacement, 2-alkoxy-4-trichloromethyl-6-alkyl-sym-triazines, were synthesized by heating the initial sym-triazines with alcohols in the presence of tertiary amines.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1674–1677, December, 1984.
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Kelarev, V.I., Dibi, A. & Lunin, A.F. Synthesis and properties of sym-triazine derivatives. 3. alkoxylation of 2-alkyl-4,6-bis(trichloromethyl)-sym-triazines containing higher alkyl radicals. Chem Heterocycl Compd 20, 1380–1384 (1984). https://doi.org/10.1007/BF00505964
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DOI: https://doi.org/10.1007/BF00505964