{"title":"Oxidation of catechol with KMnO4 by using crown ethers as phase transfer catalysts","authors":"Kazuyoshi Nakamura, Satoru Nishiyama, Shigeru Tsuruya, Mitsuo Masai","doi":"10.1016/0304-5102(94)00074-3","DOIUrl":null,"url":null,"abstract":"<div><p>The effect of crown ethers as phase transfer catalysts (PTC) was investigated in the liquid-phase oxidation of 3,5-di-<em>tert</em>-butylcatechol (3,5-DtBC) using potassium permanganate. Both the liquid—liquid (aqueous liquid layer including KMnO<sub>4</sub>/organic liquid layer including crown ether and 3,5-DtBC) and the solid—liquid (solid KMnO<sub>4</sub>/organic liquid layer including crown ether and 3,5-DtBC) systems were studied under mild reaction conditions. The oxidations of 3,5-DtBC in both systems were promoted by using crown ethers as PTCs. In the liquid—liquid system, the influence of organic solvents, acid additives and the type of crown ethers utilized were investigated. The oxidation rate of 3,5-DtBC was increased by using a solvent with a low polarity such as n-hexane and/or by adding an organic or inorganic acid to the system. Crown ethers which have a cavity that conforms to the radius of the K<sup>+</sup> ion, and were more lipophilic such as dicyclohexano-18-crown-6 (DC18C6) also caused an increase in the oxidation rate. The rate-determining step is thought to be the oxidation reaction step in the organic phase, rather than the phase transfer step of the crown ether—KMnO<sub>4</sub> complex. In the solid—liquid system, the influence of organic solvents and the type of crown ethers was investigated. The rate of 3,5-DtBC oxidation was increased by using a solvent with a high polarity such as chloroform. The complex stability between the crown ether and K<sup>+</sup> was suggested to be one of the most important factors governing the oxidation rate in the solid—liquid system.</p></div>","PeriodicalId":16567,"journal":{"name":"分子催化","volume":"93 2","pages":"Pages 195-210"},"PeriodicalIF":0.0000,"publicationDate":"1994-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0304-5102(94)00074-3","citationCount":"16","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"分子催化","FirstCategoryId":"1089","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0304510294000743","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Chemical Engineering","Score":null,"Total":0}
引用次数: 16
Abstract
The effect of crown ethers as phase transfer catalysts (PTC) was investigated in the liquid-phase oxidation of 3,5-di-tert-butylcatechol (3,5-DtBC) using potassium permanganate. Both the liquid—liquid (aqueous liquid layer including KMnO4/organic liquid layer including crown ether and 3,5-DtBC) and the solid—liquid (solid KMnO4/organic liquid layer including crown ether and 3,5-DtBC) systems were studied under mild reaction conditions. The oxidations of 3,5-DtBC in both systems were promoted by using crown ethers as PTCs. In the liquid—liquid system, the influence of organic solvents, acid additives and the type of crown ethers utilized were investigated. The oxidation rate of 3,5-DtBC was increased by using a solvent with a low polarity such as n-hexane and/or by adding an organic or inorganic acid to the system. Crown ethers which have a cavity that conforms to the radius of the K+ ion, and were more lipophilic such as dicyclohexano-18-crown-6 (DC18C6) also caused an increase in the oxidation rate. The rate-determining step is thought to be the oxidation reaction step in the organic phase, rather than the phase transfer step of the crown ether—KMnO4 complex. In the solid—liquid system, the influence of organic solvents and the type of crown ethers was investigated. The rate of 3,5-DtBC oxidation was increased by using a solvent with a high polarity such as chloroform. The complex stability between the crown ether and K+ was suggested to be one of the most important factors governing the oxidation rate in the solid—liquid system.
期刊介绍:
Journal of Molecular Catalysis (China) is a bimonthly journal, founded in 1987. It is a bimonthly journal, founded in 1987, sponsored by Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, under the supervision of Chinese Academy of Sciences, and published by Science Publishing House, which is a scholarly journal openly circulated both at home and abroad. The journal mainly reports the latest progress and research results on molecular catalysis. It contains academic papers, research briefs, research reports and progress reviews. The content focuses on coordination catalysis, enzyme catalysis, light-ribbed catalysis, stereochemistry in catalysis, catalytic reaction mechanism and kinetics, the study of catalyst surface states and the application of quantum chemistry in catalysis. We also provide contributions on the activation, deactivation and regeneration of homogeneous catalysts, solidified homogeneous catalysts and solidified enzyme catalysts in industrial catalytic processes, as well as on the optimisation and characterisation of catalysts for new catalytic processes.
The main target readers are scientists and postgraduates working in catalysis in research institutes, industrial and mining enterprises, as well as teachers and students of chemistry and chemical engineering departments in colleges and universities. Contributions from related professionals are welcome.