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Synthesis of 5-Chloroisoxazoles Derived from 2,2-Dichlorovinyl Ketones
Russian Journal of Organic Chemistry ( IF 0.8 ) Pub Date : 2021-01-11 , DOI: 10.1134/s107042802011010x A. V. Popov , V. A. Kobelevskaya , I. D. Titov , L. I. Larina , I. B. Rozentsveig
中文翻译:
2,2-二氯乙烯基酮衍生的5-氯代异恶唑的合成
更新日期:2021-01-11
Russian Journal of Organic Chemistry ( IF 0.8 ) Pub Date : 2021-01-11 , DOI: 10.1134/s107042802011010x A. V. Popov , V. A. Kobelevskaya , I. D. Titov , L. I. Larina , I. B. Rozentsveig
Abstract
The reactions of 2,2-dichlorovinyl ketones with hydroxylamine hydrochloride give the corresponding oximes. The subsequent heterocyclization of the latter under the action of t-BuOK in t-BuOH results in selective formation of 5-chloro-3-alkyl- or 5-chloro-3-aryl-substituted isoxazoles in good yields.
中文翻译:
2,2-二氯乙烯基酮衍生的5-氯代异恶唑的合成
摘要
2,2-二氯乙烯基酮与羟胺盐酸盐的反应得到相应的肟。后者随后在t- BuOH中在t- BuOK的作用下杂环化,导致以良好的产率选择性形成5-氯-3-烷基-或5-氯-3-芳基取代的异恶唑。