Guerrero-Alburquerque Natalia, Zhao Shanyu, Rentsch Daniel, Koebel Matthias M, Lattuada Marco, Malfait Wim J
Laboratory for Building Energy Materials and Components, Swiss Federal Laboratories for Materials Science and Technology, Empa, Überlandstrasse 129, 8600 Dübendorf, Switzerland.
Department of Chemistry, University of Fribourg, Chemin du Musée 9, 1700 Fribourg, Switzerland.
Polymers (Basel). 2021 May 14;13(10):1583. doi: 10.3390/polym13101583.
Ureido-functionalized compounds play an indispensable role in important biochemical processes, as well as chemical synthesis and production. Isocyanates, and KOCN in particular, are the preferred reagents for the ureido functionalization of amine-bearing compounds. In this study, we evaluate the potential of urea as a reagent to graft ureido groups onto amines at relatively low temperatures (<100 °C) in aqueous media. Urea is an inexpensive, non-toxic and biocompatible potential alternative to KOCN for ureido functionalization. From as early as 1864, urea was the go-to reagent for polyurea polycondensation, before falling into disuse after the advent of isocyanate chemistry. We systematically re-investigate the advantages and disadvantages of urea for amine transamidation. High ureido-functionalization conversion was obtained for a wide range of substrates, including primary and secondary amines and amino acids. Reaction times are nearly independent of substrate and pH, but excess urea is required for practically feasible reaction rates. Near full conversion of amines into ureido can be achieved within 10 h at 90 °C and within 24 h at 80 °C, and much slower reaction rates were determined at lower temperatures. The importance of the urea/amine ratio and the temperature dependence of the reaction rates indicate that urea decomposition into an isocyanic acid or a carbamate intermediate is the rate-limiting step. The presence of water leads to a modest increase in reaction rates, but the full conversion of amino groups into ureido groups is also possible in the absence of water in neat alcohol, consistent with a reaction mechanism mediated by an isocyanic acid intermediate (where the water assists in the proton transfer). Hence, the reaction with urea avoids the use of toxic isocyanate reagents by in situ generation of the reactive isocyanate intermediate, but the requirement to separate the excess urea from the reaction product remains a major disadvantage.
脲基官能化化合物在重要的生物化学过程以及化学合成与生产中发挥着不可或缺的作用。异氰酸酯,尤其是氰酸钾,是用于含胺化合物脲基官能化的首选试剂。在本研究中,我们评估了尿素作为一种试剂在水介质中相对低温(<100°C)下将脲基接枝到胺上的潜力。尿素是一种廉价、无毒且具有生物相容性的潜在试剂,可替代氰酸钾用于脲基官能化。早在1864年,尿素就是聚脲缩聚反应的常用试剂,在异氰酸酯化学出现后逐渐被淘汰。我们系统地重新研究了尿素用于胺转酰胺化反应的优缺点。对于包括伯胺、仲胺和氨基酸在内的多种底物,都获得了高脲基官能化转化率。反应时间几乎与底物和pH无关,但为了获得实际可行的反应速率,需要过量的尿素。在90°C下10小时内以及80°C下24小时内,胺几乎可以完全转化为脲基,而在较低温度下反应速率则慢得多。尿素/胺比例的重要性以及反应速率对温度的依赖性表明,尿素分解为异氰酸或氨基甲酸酯中间体是限速步骤。水的存在会使反应速率适度增加,但在无水的纯醇中,氨基也有可能完全转化为脲基,这与由异氰酸中间体介导的反应机理一致(其中水有助于质子转移)。因此,与尿素的反应通过原位生成活性异氰酸酯中间体避免了使用有毒的异氰酸酯试剂,但从反应产物中分离过量尿素的需求仍然是一个主要缺点。