European Journal of Chemistry

Synthesis of coumarin derivative using polymer supported reagents

Crossmark


Main Article Content

Chiheb Mhiri
Riadh Ternane
Naceur Hamdi
Lassaad Baklouti

Abstract

Recently, there has been a surge in use of polymer-supported reagents and catalysts become common tools for organic synthesis in what is known as polymer-assisted synthesis since they can simplify product isolation and purification. In this context, coumarin derivative 3 was prepared in good yield and high purity, starting from 3-methoxy salicylaldehyde, using reagents supported on a macroporous ion exchange resin. For this purpose, iminocoumarin and unsaturated nitrile were used as starting materials. The synthesized compounds were characterized by IR, NMR and mass spectrometry.


icon graph This Abstract was viewed 1611 times | icon graph Article PDF downloaded 764 times

How to Cite
(1)
Mhiri, C.; Ternane, R.; Hamdi, N.; Baklouti, L. Synthesis of Coumarin Derivative Using Polymer Supported Reagents. Eur. J. Chem. 2018, 9, 89-91.

Article Details

Share
Crossref - Scopus - Google - European PMC
References

[1]. Brahnbhatt, D. I.; Gajera, J. M.; Pandya, V. P.; Patel, M. A. Ind. J. Chem. 2007, 46(B), 869-871.

[2]. Murrey, R. D. H.; Medez, D.; Brown, S. A. The Natural coumarins occurences. Chemistry and Biochemistry, John Wiley Interscience, New York, 1982.

[3]. Bourinbaiar, A. S.; Tan, X.; Nagomy, R. Acta. Virol. 1993, 37, 241-250.

[4]. Venugopala, K. N.; Jayashree, B. S. Asian. J. Chem. 2004, 16(1), 407-411.

[5]. Luo, X.; Song, J.; Cheng, L.; Huang, D. Sci. China, Ser. B Chem. 2001, 44, 532-539.

[6]. Takadate, A.; Masuda, T.; Murata, C.; Isobe, A.; Shinohara, T.; Irikura, M.; Goya S. A. Anal. Sci. 1997, 13, 753-760.
https://doi.org/10.2116/analsci.13.753

[7]. Murata, S.; Nishimura, M.; Matsuzaki, S. Y.; Tachiya, M. Chem. Phys. Lett. 1994, 219, 200-204.
https://doi.org/10.1016/0009-2614(94)87045-4

[8]. Suppan, P. Chem. Phys. Lett. 1983, 94, 272-275.
https://doi.org/10.1016/0009-2614(83)87086-9

[9]. Nad, S.; Kumbarkar, M.; Pal, H. J. Phys. Chem. A 2003, 107, 4808-4816.
https://doi.org/10.1021/jp021543t

[10]. Kawski, A. Z. Natuforsch. A 1991, 54, 379-381.

[11]. Giri, R.; Bajaj, M. M. Curr. Sci. 1992, 62, 522-525.

[12]. Samanta, A.; Fessenden, R. W. J. Phys. Chem. A 2000, 104, 8972-8975.
https://doi.org/10.1021/jp0009960

[13]. Mhiri, C.; El Gharbi. R.; Le Bigot, Y. Synth. Commun. 1999, 29(19), 3385-3399.
https://doi.org/10.1080/00397919908085966

[14]. Cardillo, G.; Orena, M.; Porzi, G.; Sandri, S. Synthesis 1981, 793-798.
https://doi.org/10.1055/s-1981-29597

[15]. Shinkai, S.; Tsuji, H.; Hara, Y.; Manabe, O. Bull. Chem. Soc. Jpn. 1981, 54, 631-632.
https://doi.org/10.1246/bcsj.54.631

Supporting Agencies

TrendMD

Dimensions - Altmetric - scite_ - PlumX

Downloads and views

Downloads

Download data is not yet available.

Metrics

Metrics Loading ...
License Terms

License Terms

by-nc

Copyright © 2024 by Authors. This work is published and licensed by Atlanta Publishing House LLC, Atlanta, GA, USA. The full terms of this license are available at https://www.eurjchem.com/index.php/eurjchem/terms and incorporate the Creative Commons Attribution-Non Commercial (CC BY NC) (International, v4.0) License (http://creativecommons.org/licenses/by-nc/4.0). By accessing the work, you hereby accept the Terms. This is an open access article distributed under the terms and conditions of the CC BY NC License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited without any further permission from Atlanta Publishing House LLC (European Journal of Chemistry). No use, distribution, or reproduction is permitted which does not comply with these terms. Permissions for commercial use of this work beyond the scope of the License (https://www.eurjchem.com/index.php/eurjchem/terms) are administered by Atlanta Publishing House LLC (European Journal of Chemistry).