OXIDATIVE HALOGENATION OF 6-METHYLURACIL
DOI:
https://doi.org/10.1007/1117Keywords:
5, 5-dihalo-6-hydroxy-6-methyl-5, 6-dihydrouracils, 5-halo-6-methyluracils, 6-methyluracil, oxidative halogenationAbstract
An efficient method has been developed for the preparation of halo derivatives of 6-methyluracil by employing oxidative halogenation. Elemental halogens and potassium halides were used as the halogenating agents, while NaNO3 and H2O2 were used as the oxidizing agents. Iodination of 6-methyl-uracil leads to 5-iodo-6-methyluracil as the single reaction product, while bromination or chlorination lead to 5-halo-6-methyluracil, 5,5-dihalo-6-hydroxy-6-methyl-5,6-dihydrouracil, or their mixture depending on the acidity of the medium and the ratio of the substrate and reagents. Bromination of 5-chloro-6-methyluracil leads to 5-bromo-5-chloro-6-hydroxy-6-methyl-5,6-dihydrouracil, while chlorination of 6-methyl-, 5-bromo-6-methyl-, and 5-chloro-6-methyluracils using gaseous chlorine yields 5,5-dichloro-6-hydroxy-6-methyl-5,6-dihydrouracil.
Authors: V. G. Kasradze, I. B. Ignatyeva, R. A. Khusnutdinov, K. Yu. Suponitskii, M. Yu. Antipin, and M. S. Yunusov.
English Translation in Chemistry of Heterocyclic Compounds, 2012, 48 (7), pp 1018-1027
http://link.springer.com/article/10.1007/s10593-012-1094-z