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Abstract

We have studied the alkylation reactions of 2-selenoxo-6-methylpyrimidin-4-one with higher C4 -C9 alkyl halides. It was shown that the reaction proceeds mainly by the N3 and O4 reaction centers. We proved this by physicochemical method of analysis (IR, PMR, Mass)

Keywords

alkyl selenoxo pyrimidinone alkyl product

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How to Cite
Nurbaev H.I. (2023). Synthesis of selenium-containing alkyl products. Texas Journal of Engineering and Technology, 17, 33–35. Retrieved from https://zienjournals.com/index.php/tjet/article/view/3385

References

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  2. Alkylation of polyidentical anions of 2-oxo-, -thioxo-,-selenoxo-, -methylthio-, -amino-, -6-methyl-, 2-thioxo-6-phenylpyrimidinones-4 alkyl halides with C4-C9. Ph.D. in Chem. Tashkent, 1998.
  3. I.I.Grandberg Practical Works and Seminars in Organic Chemistry. Moscow V.Sh. 1978, pp. 148-149.
  4. Kh.I. Nurbayev, K.A. Zakhidov, O.E. Oripov, R.A. Samiyev, H.M. Shakhidoyatov. Tautomerism and reactivity of substituted pyrimidines. Synthesis and alkylation of 6-methyl-2-selenoxopyrimidinone-4. //Uzb.chim.zhurnal, 1996. №1-2, с 96-101.