Calcium Chloride/HCl an Efficient Co-Catalytic System for Synthesis Xanthene under Microwave Condition

Authors

  • Pramod Kulkarni Hutatma Rajguru Mahavidyalaya

DOI:

https://doi.org/10.29356/jmcs.v62i1.582

Keywords:

Calcium chloride, microwave, xanthenes, condensation reaction, β-naphthol

Abstract

Calcium chloride  along with one drop of concentrated HCl is a facile and efficient catalyst for the synthesis of aryl 14H-dibenzo[a,j] xanthene derivatives via one-pot condensation  of various substituted benzaldehydes and β-naphthol under microwave and solvent-free conditions. The advantages offered by the present protocol include shorter reaction time, good‑to‑excellent yields, operational simplicity, cost-effectiveness, and easily available catalysts.

Downloads

Download data is not yet available.

Author Biography

Pramod Kulkarni, Hutatma Rajguru Mahavidyalaya

Department of Chemistry

References

Zhu, J.; Bienaymé, H. Eds. Multicomponent Reactions Wiley-VCH: Weinheim, 2005

Dadhania, A.; Patel, V.; Raval, D. Journal of Saudi Chemical Society, 2017, 21, S163-S169.

Naidu, K. R. M.; Balam, S. K.; Mungara, A. K.; Palanisamy, A.; Shiak, I. K.; Ola, L. Molecules, 2012, 17, 7543-7555.

Poupelin, J. P.; Saint-Ruf, G.; Foussard-Blanpin, O.; Narcisse, G.; Uehida-Ernouf, G.; Lacroix, R. Eur. J. Med. Chem., 1978, 13, 67-71.

Hideo, T.; Teruomi J. Jpn. Patent 56005480, Jan 20, 1981.

Riscoe, M.; Kelly, J.; Winter, R. Current Medicinal Chemistry, 2005, 12, 2539-2549.

Pinto, M. M. M.; Sousa, M.; Nasscimento, M. S. J. Current Medicinal Chemistry, 2005, 12, 2517-2538.

Zelefack, F.; Guilet, D.; Fabre, N.; Bayet, C.; Chevalley, S.; Ngouela, S.; Lenta, B.; Valentin, A.; Tsamo, E.; Dijoux-Franca, M. J. Nat. Prod., 2009, 72, 954-957.

Saint-Ruf, G.; De, A.; Hieu, H. Bull. Chim. Ther., 1972, 7, 83-86.

Saintruf, G.; Hieu, H. T.; Poupelin, J. P. Naturwissenschaften, 1975, 62, 584-585.

Banerjee, A.; Mukherjee, A. Stain Technology, 1981, 56, 83-85.

Knight,C.; Stephens, T. Biochemical Journal, 1989, 258, 683-689.

Klimtchuk, Rodgers, M. A. J.; Neckers, D. C. J. Phys. Chem., 1992, 96, 9817-9820.

Beksert, A.; Andrieux, J.; Plat, M. Tetrahderon Lett , 1992, 33, 2805-2806.

Jha, A.; Beal, J. Tetrahedron Lett , 2004, 45, 8999-9001.

Casiraghi, G.;Casnati, G., Cornia, M. Tetrahedron Lett , 1973, 14, 679-682.

Kuo, C.; Fang, J. Synth Commun, 2001, 31, 877-892.

Knight, D.; Little, P. Synlett, 1998, 10, 1141-1143.

Ota, K.; Kito, T. Bulletin of the Chem Soc of Japan, 1976, 49, 1167-1168.

Allan, J.; Giannini, D.; Whitesides, T. J. Org. Chem. , 1982, 47, 820-823.

Papini, P.; Cimmarusti, R. Gazz. Chim. Ital, 1947, 77, 142.

Sen, R.; Sarkar, N. J. Am. Chem. Soc. , 1925, 47, 1079-1091.

Quintá, D.; Garcia, A.; Dominguez, D. Tetrahedron Lett, 2003, 44, 9291-9294.

Wang, J.; Harvey, R. Tetrahedron, 2002, 58, 5927-5931.

Sama, R. J.; Baruah, J. B. Dyes Pigment, 2005, 65, 91-92.

Khosropour,A. R.; Khodaei, M. M.; Moghannian, H. Synlett , 2005, 955-958.

Rajita, B.; Sunil Kamar, B.;Thirapathi Reddy, Y.; Narimha Reddy, P.; Sreenivasulu, N, Tetrahedron Lett, 2005, 46, 8691-8693.

Seyyedhamzeh, M.; Mirzaei, P.; Bazgir, A. Dyes Pigment, 2008, 76, 836-839.

Ziarani, G. M.; Badiei, A. –R.; Azizi, M. Scientia Iranica, 2011, 18, 455-457.

Liu, D.; Zhou, S.; Gao, J.; Li, L.; Xu, D. J. Mex. Chem. Soc., 2013, 57, 345-348.

Zolfigol, M. A.; Mossavi-Zare, A. R.; Arghavani-Hadi, P.; Zare, A.; Khakyzadeh, V.; Darvishi, G. RSC Advances, 2012, 2, 3618- 3620.

a)Cao, Y.; Yao, C.; Qin, B.; Zhang, H. Research on Chemical intermediates, 2013, 39, 3055-3062; b) Su, W.; Yang, D.; BoZhang, C. J. Tetrahedron Lett ,2008, 49, 3391-3394.

Das, B.; Ravikanth, B.; Ramu, R.; Laxminarayana, K.; Rao, B. V. J Mol. Catal. A: Chem, 2006, 225, 74-77.

Kiasat, A.; Mouradzadegun, A.; Saghanezhad, S. J. Serb. Chem. Soc., 2013, 78, 1291-1299.

Behrooz, M.; Mostafa, G.; Sepehr, Z. Bulletin of the Korean Chemical Society, 2011, 32, 1697-1702.

Nasr-Esfahani, M.; Abdizadeh, T. Rev. Roum. Chim., 2013, 58, 27-35.

Fu, G. –Y.; Huang, Y. –X.; Chen, X. –G.; Liu, X. –L. J of Chin Chem Soc, 2009, 56, 381-385.

Kumara, P. S.; Kumara, B. S.; Rajithaa, B.; Reddya, P. N.; Sreenivasulua, N.; Reddy, Y. T. ARKIVOC, 2006, 46-50 .

Gangadasu, B.; Narender, P.; Raju, B. C.; Rao, V. J. Ind. Chem., 2006, 45B, 1259-1263.

Kaboudin, B.; Zahedi, H.Chem. Lett.,2008, 37, 540-541.

Kulkarni, P.;Totawar, B.; Zubaidha, P. Monatsh Chem, 2012, 143, 625-629.

Kulkarni, P. Moroccan Journal of Chemistry, 2014, 2, 295-301.

Bhosale, D. G.; Kulkarni, P. S. Iranian Journal of Organic Chemistry, 2013, 5, 1061-1064.

Kulkarni, P. Current Microwave Chemistry, 2015, 2, 144-149.

Kulkarni, P. Journal Marocain de Chimie Hétérocyclique, 2016, 1, 71-78.

Jadhav, A.; Kulkarni, P. Der Pharma Chemica, 2017, 9, 55-58.

Kulkarni, P. Revue Roumaine De Chime, 2016, 61, 23-27.

Downloads

Published

2018-05-25

Issue

Section

Regular Articles