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Solvent-Free Synthesis of N-aryl-b-Enaminones Under Microwave Irradiation
Corresponding Author(s) : Guangyong Xie
Asian Journal of Chemistry,
Vol. 26 No. 3 (2014): Vol 26 Issue 3
Abstract
A series of N-aryl-b-enaminones were efficiently prepared by acetylacetone reacted with substituted anilines in high yields without additional solvent under microwave irradiation. The most yields can reach over 80 %. Compared with traditional routes, this method needs only 15 min and simpler after-treatment procedures while owns higher yields.
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- G.O. Dudek and R.H. Holm, J. Am. Chem. Soc., 83, 2099 (1961); doi:10.1021/ja01470a015.
- K. Ueno and A.E. Martell, J. Phys. Chem., 59, 998 (1955); doi:10.1021/j150532a002.
- G.O. Dudek and R.H. Holm, J. Am. Chem. Soc., 84, 2691 (1962); doi:10.1021/ja00873a009.
- G. Xie, Y. Li, J. Sun and C. Qian, Inorg. Chem. Commun., 12, 796 (2009); doi:10.1016/j.inoche.2009.06.012.
- R. Andres, E. de Jesus, F.J. de la Mata, J.C. Flores and R. Gómez, J. Organomet. Chem., 690, 939 (2005); doi:10.1016/j.jorganchem.2004.10.041.
- S. Gong and H. Ma, Dalton Trans., 3345 (2008); doi:10.1039/b802638f.
- H. Wang and J. Miao, Chin. J. Org. Chem, 27, 266 (2007).
- B. Rechsteiner, F. Texier-Boullet and J. Hamelin, Tetrahedron Lett., 34, 5071 (1993); doi:10.1016/S0040-4039(00)60678-0.
- H. Ai, G. Xie and L. Lei, Chem. Reagents, 32, 649 (2010) (in Chinese).
References
G.O. Dudek and R.H. Holm, J. Am. Chem. Soc., 83, 2099 (1961); doi:10.1021/ja01470a015.
K. Ueno and A.E. Martell, J. Phys. Chem., 59, 998 (1955); doi:10.1021/j150532a002.
G.O. Dudek and R.H. Holm, J. Am. Chem. Soc., 84, 2691 (1962); doi:10.1021/ja00873a009.
G. Xie, Y. Li, J. Sun and C. Qian, Inorg. Chem. Commun., 12, 796 (2009); doi:10.1016/j.inoche.2009.06.012.
R. Andres, E. de Jesus, F.J. de la Mata, J.C. Flores and R. Gómez, J. Organomet. Chem., 690, 939 (2005); doi:10.1016/j.jorganchem.2004.10.041.
S. Gong and H. Ma, Dalton Trans., 3345 (2008); doi:10.1039/b802638f.
H. Wang and J. Miao, Chin. J. Org. Chem, 27, 266 (2007).
B. Rechsteiner, F. Texier-Boullet and J. Hamelin, Tetrahedron Lett., 34, 5071 (1993); doi:10.1016/S0040-4039(00)60678-0.
H. Ai, G. Xie and L. Lei, Chem. Reagents, 32, 649 (2010) (in Chinese).