Environmentally Friendly Syntheses of Imines Applying the Pressure Reduction Technique: Reaction Cases of Less Reactive Amines and Studies by Computational Chemistry

Shoko Suzuki, Hiroyuki Ito, M. Noike, S. Ishizuka, R. Nonaka, K. Funaki, T. Kodama, S. Sakaki, T. Nishino, Mina Ito, Toranosuke Takahasi, Y. Yokoyama*
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Abstract

Recently, the development of environmentally friendly syntheses of imine derivatives, which were attracting great attention for their reactivity and structure in various fields, progressed rapidly because the concept of green chemistry had deeply penetrated into society. In our previous work, we had reported new synthetic methods of imine derivatives using some active amines under solvent- and catalyst-free reaction conditions. This synthetic reaction proceeded smoothly and target compounds were obtained in excellent yields. In this system, when less reactive amines were used as substrates, the synthetic reaction was not finished in the short reaction time, and the corresponding compounds were given in moderate yields. In order to solve this point, we tried to improve the reaction conditions of this method. Through this improvement, it was found that pure target compounds could be obtained in excellent yields by using 1.1 equivalents of less reactive amines to aldehydes and extending the reaction time compared with our previous work. In this paper, we will introduce the detail of this study, and also report the result of the investigation of the reaction property by computational chemistry.
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应用减压技术环境友好合成亚胺:低反应性胺的反应案例及计算化学研究
近年来,由于绿色化学的理念深入社会,亚胺衍生物的环境友好合成技术发展迅速,因其反应性和结构受到各个领域的广泛关注。在我们之前的工作中,我们报道了在无溶剂和无催化剂的条件下,利用一些活性胺合成亚胺衍生物的新方法。该合成反应进行顺利,目标化合物收率高。在该体系中,当使用活性较低的胺作为底物时,合成反应不能在较短的反应时间内完成,相应化合物的产率也不高。为了解决这一问题,我们尝试改善该方法的反应条件。通过这一改进,发现与我们之前的工作相比,使用1.1等量的胺对醛的反应性降低,并延长反应时间,可以获得纯度较高的目标化合物。在本文中,我们将详细介绍这一研究的细节,并报告了用计算化学方法研究反应性质的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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