Synthesis of Oxaazaisowurtzitane Derivatives Via Condensation of p-Toluenesulfonamide With Glyoxal

IF 2 3区 化学 Q2 CHEMISTRY, ORGANIC Journal of Heterocyclic Chemistry Pub Date : 2024-08-27 DOI:10.1002/jhet.4885
Artyom E. Paromov, Valentina А. Kubasova, Sergey V. Sysolyatin
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Abstract

This work presents the study results on the acid-catalyzed cascade condensation of p-toluenesulfonamide with glyoxal in H2SO4 in order to synthesize aza- and oxaazaisowurtzitanes—a platform for promising high-energy-density compounds—and explore their formation processes. The effects of the ratio of starting reactants, acidity, reaction medium concentration, and temperature on this process were studied in detail. Five novel compounds were derived, including four oxaazaisowurtzitanes comprising one to three aza groups, and one condensation intermediate. The most favorable conditions for the formation of the resultant caged compounds were established and some new regularities of the process were revealed. For instance, the reaction medium concentration was discovered for the first time to influence the generation process of oxaazaisowurtzitanes via direct condensation. The limiting stage of the cage formation process of oxaazaisowurtzitanes was identified. The formation rate of the oxaazaisowurtzitanes was shown to be dependent on their structure. The factor dramatically reducing the yield of the oxaazaisowurtzitanes at elevated synthesis temperature was also revealed.

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通过对甲苯磺酰胺与乙二醛缩合合成噁唑烷-乌齐坦衍生物
本研究介绍了对甲苯磺酰胺与乙二醛在 H2SO4 中进行酸催化级联缩合的研究成果,目的是合成氮杂和噁氮昭乌坦--一种有前途的高能量密度化合物的平台--并探索其形成过程。我们详细研究了起始反应物的比例、酸度、反应介质浓度和温度对这一过程的影响。研究得出了五种新型化合物,包括四种由一至三个氮杂基团组成的噁唑-艾素乌坦和一种缩合中间体。研究确定了生成这些笼状化合物的最有利条件,并揭示了这一过程的一些新规律。例如,研究人员首次发现反应介质浓度会影响通过直接缩合生成噁唑烷的过程。确定了噁唑麝香石竹笼形成过程的极限阶段。研究表明,噁唑麝香檀的形成速率取决于其结构。此外,还揭示了在合成温度升高的情况下显著降低噁唑脲玳烷产量的因素。
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来源期刊
Journal of Heterocyclic Chemistry
Journal of Heterocyclic Chemistry 化学-有机化学
CiteScore
5.20
自引率
4.20%
发文量
177
审稿时长
3.9 months
期刊介绍: The Journal of Heterocyclic Chemistry is interested in publishing research on all aspects of heterocyclic chemistry, especially development and application of efficient synthetic methodologies and strategies for the synthesis of various heterocyclic compounds. In addition, Journal of Heterocyclic Chemistry promotes research in other areas that contribute to heterocyclic synthesis/application, such as synthesis design, reaction techniques, flow chemistry and continuous processing, multiphase catalysis, green chemistry, catalyst immobilization and recycling.
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