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铜(I)/离子液体在室温下促进二氧化碳转化为恶唑烷酮。

Cu(I)/Ionic Liquids Promote the Conversion of Carbon Dioxide into Oxazolidinones at Room Temperature.

机构信息

Collaborative Innovation Center of Henan Province for Green Manufacturing of Fine Chemicals, Key Laboratory of Green Chemical Media and Reactions, Ministry of Education, School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang, Henan 453007, China.

College of Chemical and Environmental Engineering, Shandong University of Science and Technology, Qingdao 266590, Shandong, China.

出版信息

Molecules. 2019 Mar 29;24(7):1241. doi: 10.3390/molecules24071241.

DOI:10.3390/molecules24071241
PMID:30934963
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6480545/
Abstract

Recently, the efficient chemical fixation of carbon dioxide (CO₂) into high value chemicals without using noble metal catalysts has become extremely appealing from the viewpoint of sustainable chemistry. In this work, a one-pot three component reaction of propargylic alcohols, anines and CO₂ that can proceed in an atom economy and environmentally benign manner by combination of CuI and tetrabutylphosphonium imidazol ([P][Im]) as a catalyst was described. Catalysis studies indicate that this catalytic system is an effective catalyst for the conversion of CO₂ into oxazolidinones at room temperature and ambient pressure without any solvent. The results provide a useful way to design novel noble metal-free catalyst systems for the transformation of CO₂ into other valuable compounds.

摘要

最近,从可持续化学的角度来看,高效地将二氧化碳(CO₂)化学固定为高价值化学品而不使用贵金属催化剂变得极具吸引力。在这项工作中,描述了炔丙醇、苯胺和 CO₂的一锅三组分反应,该反应可以通过 CuI 和四丁基膦咪唑([P][Im])的组合以原子经济性和环境友好的方式进行。催化研究表明,该催化体系是在室温常压下将 CO₂转化为恶唑烷酮的有效催化剂,无需任何溶剂。该结果为设计新型无贵金属催化剂体系将 CO₂转化为其他有价值的化合物提供了有用的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d1e/6480545/2c92ff6918ea/molecules-24-01241-sch003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d1e/6480545/fb7c050a1a4d/molecules-24-01241-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d1e/6480545/a6785a6b59ae/molecules-24-01241-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d1e/6480545/03d9b8e40ef7/molecules-24-01241-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d1e/6480545/04bdb7107a25/molecules-24-01241-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d1e/6480545/5b3352aa700b/molecules-24-01241-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d1e/6480545/85bebc3bcb4a/molecules-24-01241-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d1e/6480545/2c92ff6918ea/molecules-24-01241-sch003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d1e/6480545/fb7c050a1a4d/molecules-24-01241-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d1e/6480545/a6785a6b59ae/molecules-24-01241-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d1e/6480545/03d9b8e40ef7/molecules-24-01241-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d1e/6480545/04bdb7107a25/molecules-24-01241-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d1e/6480545/5b3352aa700b/molecules-24-01241-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d1e/6480545/85bebc3bcb4a/molecules-24-01241-sch002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d1e/6480545/2c92ff6918ea/molecules-24-01241-sch003.jpg

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本文引用的文献

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Imidazolium-Salt-Functionalized Covalent Organic Frameworks for Highly Efficient Catalysis of CO Conversion.用于高效催化CO转化的咪唑盐功能化共价有机框架
ChemSusChem. 2019 Jun 7;12(11):2421-2427. doi: 10.1002/cssc.201900570. Epub 2019 May 2.
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Challenges in the Greener Production of Formates/Formic Acid, Methanol, and DME by Heterogeneously Catalyzed CO Hydrogenation Processes.多相催化CO加氢过程中绿色生产甲酸盐/甲酸、甲醇和二甲醚的挑战。
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Ag /TMG-Promoted Cascade Reaction of Propargyl Alcohols, Carbon Dioxide, and 2-Aminoethanols to 2-Oxazolidinones.
银/四甲基胍促进的炔丙醇、二氧化碳和2-氨基乙醇合成2-恶唑烷酮的串联反应
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Efficient Ionic-Liquid-Promoted Chemical Fixation of CO into α-Alkylidene Cyclic Carbonates.离子液体高效促进CO化学固定合成α-亚烷基环碳酸酯
ChemSusChem. 2017 Mar 22;10(6):1120-1127. doi: 10.1002/cssc.201601129. Epub 2016 Oct 28.
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Auto-Tandem Catalysis in Ionic Liquids: Synthesis of 2-Oxazolidinones by Palladium-Catalyzed Oxidative Carbonylation of Propargylic Amines in EmimEtSO₄.离子液体中的自串联催化:在1-乙基-3-甲基咪唑硫酸乙酯中通过钯催化的炔丙基胺氧化羰基化反应合成2-恶唑烷酮
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Chem Commun (Camb). 2016 Jun 14;52(50):7830-3. doi: 10.1039/c6cc02853e.
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