J. Iran. Chem. Soc., Vol. 5, No. 1 March 2008, pp.100~105.
Current location: JICS Archive > Vol. 5 > No. 1 > Articles : 11
A Solventless Protocol for the Michael Addition of Aromatic Amides to α,β-Unsaturated Esters Promoted by Microwave Irradiation
A. Zarea,*, A. Hasaninejadb,*, A. Khalafi-Nezhadc, A. Parhamic and A.R. Moosavi Zarec
aDepartment of Chemistry, Payame Nour University of Bushehr, Bushehr 1698, Iran
bDepartment of Chemistry, Faculty of Sciences, Persian Gulf University, Bushehr 75169, Iran
cDepartment of Chemistry, College of Sciences, Shiraz University, Shiraz 71454, Iran
A very simple and efficient solvent-free method for the preparation of N-benzoylated β-amino esters (protected β-amino acids) via the microwave-assisted Michael addition of aromatic amides to α,β-unsaturated esters in the presence of Cs2CO3 and tetrabutylammonium bromide (TBAB) is described. The advantages of this method are efficiency, high yields and short reaction times.
Keywords: Michael addition,Amide, α,β-Unsaturated ester, Microwave, Protected β-amino acid
