首页 | 本学科首页   官方微博 | 高级检索  
     检索      


Microwave assisted IMDAF# reaction: Microwave irradiation applied with success to cycloaddition reaction of N-propargyl-N-p-tolyl-N-2-furfurylamines
Authors:Ana Dunja Mance  Krešimir Jakopčić
Institution:(1) Faculty of Chemical Engineering and Technology, Department of Organic Chemistry, University of Zagreb, Marulicacuteev trg 20, Zagreb, Croatia
Abstract:The new tertiary furfurylamine with triple bond as a dienophylic part i. e. N-(5-methyl-2-furfuryl)-N-prop-2-ynyl-p-toluidine (1) was prepared and the intramolecular Diels-Alder reaction of the amine (1) was performed under microwave irradiation conditions and by heating a benzene solution of the amine under nitrogen. Comparing the results of the usual thermal and the MAOS reaction, we confirmed our expectations that MAOS could promote the outcome of IMDA reaction of the suitably N-substituted tertiary 2-furfuryl-amines. In the present example, N-p-tolyl-5-methyl-5,7a-dihydro-5,7a-epoxyisoindoline was obtained in much better yield and of higher purity.The acronym for: Intramolecular Diels-Alder Reaction of Furan.The acronym for: Microwave-Assisted Organic Synthesis.
Keywords:alkynylarylfurfurylamine  [4+2]cycloaddition  epoxyisoindoline  IMDAF#  MAOS##
本文献已被 SpringerLink 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号