Department of Chemistry, University of Oxford, Oxford, UK.
Department of Chemistry, Indian Institute of Technology, Kanpur, India.
Nat Protoc. 2024 Aug;19(8):2358-2385. doi: 10.1038/s41596-024-00978-0. Epub 2024 Apr 25.
Methanol is a key building block in the chemical industry. In recent years, it has been used as a C1 source in various organic transformations in the presence of a transition-metal catalyst. This protocol describes the ruthenium- and cobalt-catalyzed utilization of methanol in different types of methylation reactions and heterocycle synthesis. Initially, we describe the synthesis of tridentate ligands (L1-L3) and their corresponding Ru(II) complexes (Ru-1, -2 and -3) and then detail how to apply these Ru(II) complexes and Co/PP (PP = P(CHCHPPh)) in various methanol dehydrogenative coupling reactions. We discuss six types of transformations by using methanol or a methanol/water mixture. The experimental setup for all the catalytic reactions is similar and involves adding all the respective reagents and solvents to an argon-filled pressure tube, which is sealed (by screw cap) and refluxed at the indicated temperature before the desired products are isolated and characterized. The catalytic systems described in this protocol work well for both small-scale and preparative-scale synthesis of various N-methylated amines/amides, C-methylated products and quinazolinones. These catalytic reactions are greener and more sustainable than conventional synthesis methods, with only H and/or HO as by-products, and we evaluate the 'green chemistry metrics' for a typical substrate. The total time required for the catalytic experiments described in this protocol is 16-28 h, and the operation time is 4 h. An average level of expertise in organic synthesis is required to carry out these protocols.
甲醇是化学工业的重要基石。近年来,在过渡金属催化剂的存在下,甲醇被用作各种有机转化中的 C1 源。本方案描述了在不同类型的甲基化反应和杂环合成中使用甲醇的钌和钴催化作用。最初,我们描述了三齿配体(L1-L3)及其相应的 Ru(II) 配合物(Ru-1、-2 和 -3)的合成,然后详细说明了如何应用这些 Ru(II) 配合物和 Co/PP(PP = P(CHCHPPh)) 在各种甲醇脱氢偶联反应中。我们通过使用甲醇或甲醇/水混合物讨论了六种类型的转化。所有催化反应的实验装置相似,包括将所有相应的试剂和溶剂添加到充满氩气的压力管中,将其密封(用螺旋盖)并在所需产物被分离和表征之前在指定温度下回流。本方案中描述的催化体系适用于各种 N-甲基化胺/酰胺、C-甲基化产物和喹唑啉酮的小规模和中试规模合成。与传统合成方法相比,这些催化反应更加环保和可持续,仅产生 H 和/或 HO 作为副产物,我们还评估了典型底物的“绿色化学指标”。本方案中描述的催化实验所需的总时间为 16-28 小时,操作时间为 4 小时。需要具备一定的有机合成专业知识才能进行这些方案。