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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
Affiliation:(1) Faculty of Chemical Engineering and Technology, Department of Organic Chemistry, University of Zagreb, Maruli"cacute"ev 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##
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