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dc.contributor.authorThiti Junpiromen_US
dc.contributor.authorPraput Thavornyutikarnen_US
dc.contributor.authorPuttinan Meepowpanen_US
dc.date.accessioned2019-05-07T09:59:50Z-
dc.date.available2019-05-07T09:59:50Z-
dc.date.issued2018en_US
dc.identifier.issn0125-2526en_US
dc.identifier.urihttp://it.science.cmu.ac.th/ejournal/dl.php?journal_id=9334en_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/64171-
dc.description.abstractTwo AlCl3 supported imidazolium salts (1, 2) were prepared and utilized as the catalysts for the acylation of anisole. The standard conditions for the reaction were optimized. The acylation of anisole using those AlCl3 supported imidazolium provided the desired product in high percentage yield in a short period of time. The results revealed that AlCl3 supported imidazolium salts are suitable for this reaction when the molar ratio of AlCl3: imidazolium is 2:1 and the reaction smoothly proceeded even at the low temperature such as 0 oC. Moreover, the AlCl3-supported catalyst 1 demonstrated the promising reusability after being catalytically used for 3 times without losing properties.en_US
dc.languageEngen_US
dc.publisherScience Faculty of Chiang Mai Universityen_US
dc.titleThe Catalytic Investigation of Supported Imidazolium-chloroaluminate (AlCl3-lLs) in Friedel-Craft Acylation of Anisoleen_US
dc.typeบทความวารสารen_US
article.title.sourcetitleChiang Mai Journal of Scienceen_US
article.volume45en_US
article.stream.affiliationsDepartment of Chemistry, Faculty of Science, Chiang Mai University, Chiang Mai, 50200 Thailand.en_US
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