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非均相金属有机框架催化下sp C-H键的辅助导向醚化反应:乙磺酰胺的合成

Auxiliary-directed etherification of sp C-H bonds under heterogeneous metal-organic framework catalysis: synthesis of ethenzamide.

作者信息

Tran Chau B, Duong Xuan N T, Lu Huy D, Cao Thu T V, Truong Thanh

机构信息

Department of Chemical Engineering, Ho Chi Minh University of Technology, VNU-HCM 268 Ly Thuong Kiet, District 10 Ho Chi Minh City Viet Nam

出版信息

RSC Adv. 2018 Jan 16;8(5):2829-2836. doi: 10.1039/c7ra12010a. eCollection 2018 Jan 9.

Abstract

An efficient protocol for 8-aminoquinoline assisted alkoxylation and phenoxylation of sp C-H bonds under heterogeneous catalysis was developed. The optimal conditions employed Cu-MOF-74 (20%), KCO base, pyridine ligand or dimethyl formamide solvent, and O oxidant at 80 °C or 100 °C for 24 hours. Cu-MOF-74 revealed remarkably higher activity when compared with other previously commonly used Cu-MOFs in cross coupling reactions, supported copper catalysts, and homogeneous copper salts. The reaction scope with respect to coupling partners included a wide range of various substrates. Interestingly, the developed conditions are applicable for the synthesis of high-profile relevant biological agents from easily accessible starting materials. Furthermore, a leaching test confirmed the reaction heterogeneity and the catalyst was reused and recycled at least 8 times with trivial degradation in activity.

摘要

开发了一种在多相催化下8-氨基喹啉辅助sp C-H键的烷氧基化和苯氧基化的有效方案。最佳条件是使用20%的Cu-MOF-74、KCO碱、吡啶配体或二甲基甲酰胺溶剂,以及O氧化剂,在80℃或100℃下反应24小时。与其他先前常用于交叉偶联反应的Cu-MOFs、负载型铜催化剂和均相铜盐相比,Cu-MOF-74显示出显著更高的活性。关于偶联伙伴的反应范围包括各种不同的底物。有趣的是,所开发的条件适用于从易于获得的起始原料合成备受关注的相关生物制剂。此外,浸出试验证实了反应的非均相性,并且催化剂至少重复使用和循环8次,活性仅有轻微下降。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab39/9077472/41481e153aed/c7ra12010a-f1.jpg

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