苯胺和 1-(取代的亚苄基)-2-苯基肼亲电硫氰酸化的高效环保程序

Chemistry Pub Date : 2024-06-10 DOI:10.3390/chemistry6030027
A. Mallikarjunaswamy, Gouthami Kuruvalli, K. Syed, Vaddi Damodara Reddy, Vipin A. Nair
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引用次数: 0

摘要

硫氰酸盐是一类重要的有机化合物,常见于天然产品中,具有出色的抗菌活性。亲电硫氰酸化是在母体有机分子中引入 -SCN 官能团的最有效方法之一。在这项工作中,我们利用市售的 N-溴琥珀酰亚胺(NBS)和硫氰酸钾(KSCN),探索了一种环保、高效的苯胺和 1-(取代亚苄基)-2-苯肼硫氰酸化方法。与现有方法相比,优化后的方案以良好的区域选择性和极高的产率获得了硫氰酸盐。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An Efficient and Eco-Friendly Procedure for Electrophilic Thiocyanation of Anilines and 1-(Substituted benzylidene)-2-phenyl Hydrazines
Thiocyanates form an important class of organic compounds commonly found in natural products that exhibit excellent antimicrobial activity. The electrophilic thiocyanation is one of the most effective methods of introducing a -SCN functional group to the parent organic molecule. In this work, we explored an eco-friendly and highly efficient method for thiocyanation of anilines and 1-(substituted benzylidene)-2-phenylhydrazines using commercially available N-bromoscuccinimide (NBS) and potassium thiocyanate (KSCN). The optimized protocol afforded thiocyanates with good regioselectivity and excellent yields in comparison to the available methods.
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