Cyanuric Chloride Derivatives. VII. Transesterification Reactions of Alkoxy-s-triazines. Polyammelide Ethers

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Abstract

Transesterification has been investigated as a preparative method for monomeric and polymeric alkoxy- and alkoxyamino-s-triazines. Both classes undergo transesterification reactions with primary or secondary alcohols in the presence of catalytic amounts of sodium alkoxides. This affords a method of preparation for those derivatives which cannot be prepared directly from the corresponding chloro-s-triazines. Linear polyammelide esters have been prepared by transesterification of 2-amino-4,6-dialkoxy-s-triazines with glycols. The effects of structural modifications and conditions of reaction are discussed. © 1951, American Chemical Society. All rights reserved.

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Dudley, J. R., Thurston, J. T., Schaefer, F. C., Hull, C. J., Holm-Hansen, D., & Adams, P. (1951). Cyanuric Chloride Derivatives. VII. Transesterification Reactions of Alkoxy-s-triazines. Polyammelide Ethers. Journal of the American Chemical Society, 73(7), 2999–3004. https://doi.org/10.1021/ja01151a007

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