European Journal of Chemistry

Synthesis of coumarin derivative using polymer supported reagents

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Published: Jun 30, 2018
DOI: https://doi.org/10.5155/eurjchem.9.2.89-91.1691
Keywords:
Iminocoumarin, Selective synthesis, Unsaturated nitrile, Knoevenagel condensation, 3-Methoxy salicylaldehyde, Polymer supported reagent
Section
Research Article
Issue
Vol. 9 No. 2 (2018): June 2018
Dates
Received 2018-03-01
Accepted 2018-03-31
Published 2018-06-30
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Chiheb Mhiri
Laboratory of Applied Chemistry and Natural Substances Resources and Environment, Faculty of Sciences, University of Carthage, Zarzouna‐Bizerta, 7021, Tunisia
http://orcid.org/0000-0001-6331-6393
Riadh Ternane
Laboratory of Applied Chemistry and Natural Substances Resources and Environment, Faculty of Sciences, University of Carthage, Zarzouna‐Bizerta, 7021, Tunisia
http://orcid.org/0000-0003-3557-7558
Naceur Hamdi
Chemistry Department, College of Science and Arts, Qassim University, Al-Rass, 51921, Kingdom of Saudi Arabia
http://orcid.org/0000-0003-0110-9588
Lassaad Baklouti
Laboratory of Applied Chemistry and Natural Substances Resources and Environment, Faculty of Sciences, University of Carthage, Zarzouna‐Bizerta, 7021, Tunisia
http://orcid.org/0000-0002-5142-7501

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.


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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.

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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

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