Eggshell Waste : An Efficient Solid Catalyst for the Synthesisof 5-Arylidene Barbituric Acids under Solvent-Free Condition
Keywords:
Chicken eggshell waste, 5-Arylidene barbituric acid derivatives, Green catalyst, Grinding, Solvent free condition.Abstract
Efficient synthesis of 5-arylidene barbituric acid derivatives in presence of chicken eggshell waste at room temperature with grinding has been reported. Biologically active 5-arylidene barbituric acid derivatives were obtained in high yields (88-96 %) in a short reaction time (2-7 min) under solvent-free condition. This method has advantages such as avoidance of the organic solvents, short reaction times and production of pure products without any by product.
References
- J T. Bojarski, J. L. Mokrosz, H. J. Barton, M. H. Paluchowska, Adv. Heterocycl. Chem.,38 (1985) 229.
- F H. Ali Bamanie, A. S. Shehata, M. A. Moustafa, M. M. Mashaly, J. American Sci.,8 (2012) 481.
- A H. Shamroukh, M. E. Zaki, E. M.Morsy, F. M. Abdel-Motti, F. M. E. Abdel-Megeid, Arch. Pharm. (Weinheim)., 340 (2007) 236.
- I O. Zhuravel, S. A. Grashenkova, L. V. Yakovleva, O. V. Borisov, S. M. Kovalenko,V. P. Chernikh,Zh. Org. Khim., 4 (2006) 25.
- V K. Ahluwalia, R. Batla, A. Khurana, R. Kumar, Ind. J. Chem. B., 29 (1990) 1141.
- Y Frangin, C.Guimbal, F. Wissocq, H. Zamarlik, Synthesis, 12 (1986) 1046.
- K Tanaka, X.Chen, F. Yoneda,Tetrahedron, 44 (1988) 3241.
- J D. Figueroa-Villar,C. E. Rangel, L. N. Dos Santos,Synth. Commun., 22 (1992) 1159.
- M C. Rezende, P. Campodonico, E.Abuin, J. Kossanyi, Spectrochim. Acta A., 57 (2001) 1183.
- K Tanaka, X. Chen, T. Kimura, F. Yoneda, Tetrahedron Lett., 28 (1987) 4173.
- K Tanaka, X. Chen, T. Kimura, F. Yoneda, Chem. Pharm. Bull., 34 (1986) 3945.
- J T. Li, H. G. Dai, D. Liu, T. S. Li, Synth. Commun., 36 (2006) 789.
- S K. Dewan, R. Singh, Synth. Commun., 33 (2003) 3085.
- J R. Rajput, G. Kaur, Chin. J. Catal., 34 (2013) 1697.
- C Wang, J. Ma, X. Zhou, X. Zang, Z. Wang, Y. Gao, P. Cui, Synth. Commun., 35 (2005) 2759.
- G Alcerreca, R. Sanabria, R. Miranda, G. Arroyo, J. Tamariz, F. Delgado, Synth. Commun.,30 (2000) 1295.
- J M. Khurana, K.Vij, Catal. Lett., 138 (2010) 104.
- A Venkat Narsaiah, K. Nagaiah, Synth. Commun., 33 (2003) 3825.
- F Bigi, M. L. Conforti, R. Maggi, A. Piccinno, G. Sartori, Green Chem., 2 (2000) 101.
- M L. Deb, P. J. Bhuyan, Tetrahedron Lett., 46 (2005) 6453.
- J Lu, Y. Li, Y.Bai, M. Tian, Heterocycles, 63 (2004) 583.
- Y Hu, Z. C. Chen, Z. G. Le, Q. G.Zheng, Synth. Commun., 34 (2004) 4521.
- J H. Clark, Green Chem., 1 (1999) 1.
- A V. Borhade, B. K. Uphade, A. G. Gadhave, Res. Chem. Intermed., 42 (2016) 6301.
- A V. Borhade, B. K. Uphade, J. Iran. Chem. Soc., 12 (2015) 1107
- A V. Borhade, B. K.Uphade, D. R.Tope, Res. Chem. Intermed., 40 (2014) 211.
- A V. Borhade, B. K.Uphade, D. R. Tope, J. Chem. Sci., 125 (2013) 583.
- A V. Borhade, B. K.Uphade, A. G. Gadhave, Res. Chem. Intermed., 41 (2015) 1447.
- A V. Borhade,B. K. Uphade, Iranian J. Catalysis, 6 (2016) 197.
- A Dandia, V. Parewa, S. L. Gupta, K. S. Rathore, J. Mol. Catal. A.Chem., 373 (2013) 61.
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