N-(1-羟基丁烷-2-基)-4-硝基苯磺酰胺:一种一锅合成α-氨基膦酸盐的新型有机催化剂

IF 2.5 Q2 CHEMISTRY, MULTIDISCIPLINARY
Swati Jaydeokar , Vikas G. Yadav , Priyanka V. Bandivadekar , Ganesh Chaturbhuj , Vijaykumar L. Chavan
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引用次数: 0

摘要

本研究重点研究了芳香醛/酮、胺和亚磷酸二烷基酯一锅三组分反应制备α-氨基膦酸盐的高效方法。该反应由新型有机催化剂N-(1-羟基丁烷-2-基)-4-硝基苯磺酰胺催化。SO2-NH基团用于卡巴尼克场反应,提高了催化剂的酸度。当前方法的主要优点包括廉价、无毒、高效的有机催化剂、产率高、反应时间短、溶剂环保、实验方法简单、后处理步骤简单、催化剂适用于广泛的底物范围。所有芳香族、杂环醛和环酮变体都能有效地反应,在较短的反应时间内产生更高产率的α-氨基膦酸盐(26)。此外,催化剂很容易回收并在几个循环中重复使用,而不会显著降低效率。这提供了经济和环境效益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

N-(1-hydroxybutan-2-yl)-4-nitrobenzene sulfonamide: A novel organocatalyst for an effective one-pot synthesis of α-amino phosphonates

N-(1-hydroxybutan-2-yl)-4-nitrobenzene sulfonamide: A novel organocatalyst for an effective one-pot synthesis of α-amino phosphonates
This study emphasizes an efficient method for a one-pot, three-component reaction of aromatic aldehyde/ketone, amines, and dialkyl phosphite to produce α-Amino phosphonates. This reaction was catalyzed by a novel organocatalyst N-(1-hydroxybutan-2-yl)-4-nitrobenzene sulfonamide. The acidity of the synthesized catalyst was increased due to SO2-NH group which was used in Kabachnik Field reaction. The main advantages of the current method include inexpensive, non-toxic, efficient organo catalyst, high yields, a reduced reaction time, green solvent, an easy experimental method, a simple workup procedure, and the suitability of the catalyst to withstand a wide range of substrate scope All aromatic, heterocyclic aldehydes and cyclic ketone variations reacted effectively producing greater yields of the respective α-amino phosphonates in a shorter reaction time (26) examples. Additionally, the catalyst was easily recovered and reused over several cycles without significantly decreasing effectiveness. This provides economic and environmental benefits.
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来源期刊
Results in Chemistry
Results in Chemistry Chemistry-Chemistry (all)
CiteScore
2.70
自引率
8.70%
发文量
380
审稿时长
56 days
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