Journal2014

Tandem Knoevenagel–Michael-cyclocondensation reactions of malononitrile, various aldehydes and dimedone using acetic acid functionalized ionic liquid

Ahmad Reza Moosavi‐Zare, Mohammad Ali Zolfigol, Omid Khaledian, Vahid Khakyzadeh, Majid D. Farahani, Hendrik G. Kruger

New Journal of Chemistry Vol. 38, No. 6, 2342–2342

چکیده

An efficient solvent-free protocol for the synthesis of tetrahydrobenzo[b]pyrans by the condensation of malononitrile, dimedone and various aldehydes in the presence of acetic acid functionalized imidazolium salts (1-carboxymethyl-3-methylimidazolium bromide {[cmmim]Br} and 1-carboxymethy1-3-methylimidazolium tetrafluoroborate {[cmmim][BF4]}) as reusable catalysts has been reported. The turn over frequency (TOF) values of the catalysts are higher than some of the previously reported catalysts. Also, thermal gravimetric analysis (TGA), differential thermal gravimetry (DTG), X-ray diffraction analysis (XRD) and calculations of the size and inter-planer distance of the catalysts have been reported in this work.

موضوعات و کلیدواژه‌ها

Multicomponent Synthesis of HeterocyclesIonic liquids properties and applicationsSynthesis and biological activityDimedoneMalononitrileChemistryIonic liquidKnoevenagel condensationTetrafluoroborateCatalysisAcetic acidThermogravimetric analysisOrganic chemistryBromideAcetic anhydride

ارجاع علمی

Ahmad Reza Moosavi‐Zare, Mohammad Ali Zolfigol, Omid Khaledian, Vahid Khakyzadeh, Majid D. Farahani, Hendrik G. Kruger. “Tandem Knoevenagel–Michael-cyclocondensation reactions of malononitrile, various aldehydes and dimedone using acetic acid functionalized ionic liquid.” New Journal of Chemistry, 2014. https://doi.org/10.1039/c3nj01509b