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Current Microwave Chemistry

Editor-in-Chief

ISSN (Print): 2213-3356
ISSN (Online): 2213-3364

Review Article

Conventional vs. Microwave-assisted Synthesis: A Comparative Study on The Synthesis of Tri-substituted imidazoles

Author(s): Tanvi Goel, Deepali Bansode* and Naman Vijaykumar Jain

Volume 9, Issue 2, 2022

Published on: 27 January, 2023

Page: [105 - 108] Pages: 4

DOI: 10.2174/2213335610666230105154742

Price: $65

Abstract

Background: The organic and peptide synthesis, various nanotechnology, and biochemistry processes are being carried out using microwave irradiation. The use of microwaves for synthesis has increased in the past two decades. The microwave offers several advantages such as ease of handling, lesser reaction times, quality of the product, and eco-friendly, which is green. The conventional method of synthesis, on the other hand, requires a longer time, is difficult to handle and maintenance of temperature is also difficult. The use of microwave-assisted reactions over conventional methods is advantageous in medicinal chemistry research as they will be less timeconsuming and crucial in drug discovery and development. On the other side, they might not work in bulk synthesis due to their limited capacity for loading the reaction mixture.

Objective: The present work aims to compare reaction time, temperature and percentage of yield of the microwave-assisted synthesis method against the conventional method.

Methods: A novel, simple, and green method was developed for the synthesis of tri-substituted imidazoles by microwave irradiation. Both derivatives from conventional and microwave-assisted synthesis were characterized by IR spectroscopy, Mass spectrometry, and 1H-NMR spectroscopy. The same derivatives were also synthesized by the conventional method for comparison.

Results: A comparison of both methods was made by comparing the reaction time and the percentage yield. It was found that microwave-assisted reactions produced greater yield in the minimal time, though at different reaction temperatures.

Conclusion: It can be concluded from the present comparison study that the use of the microwave for synthesis provides numerous advantages; thus, newer molecules are developed quickly anthat are developed quickly. To further proceed in this direction and to produce evidences, synthesis of more derivatives may be required. The only disadvantage is that it cannot be used for bulk synthesis of the compounds.

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Graphical Abstract

[1]
Zaręba, P.; Drabczyk, A.K.; Wnorowski, A.; Pindelska, E.; Latacz, G.; Jaśkowska, J. Eco-friendly methods of synthesis and preliminary biological evaluation of sulfonamide derivatives of cyclic arylguanidines. Ultrason. Sonochem., 2022, 90(9), 106165.
[http://dx.doi.org/10.1016/j.ultsonch.2022.106165] [PMID: 36183548]
[2]
Kumar, A.; Kuang, Y.; Liang, Z.; Sun, X. Microwave chemistry, recent advancements, and eco-friendly microwave-assisted synthesis of nanoarchitectures and their applications: a review. Materials Today Nano, 2020, 11100076.
[http://dx.doi.org/10.1016/j.mtnano.2020.100076]
[3]
Kaur, N. Advances in Microwave-Assisted Synthesis for Five-Membered N -Heterocycle Synthesis. Synth. Commun., 2015, 45(4), 432-457.
[http://dx.doi.org/10.1080/00397911.2013.824982]
[4]
Nüchter, M.; Ondruschka, B.; Bonrath, W.; Gum, A. Microwave assisted synthesis – a critical technology overview. Green Chem., 2004, 6(3), 128-141.
[http://dx.doi.org/10.1039/B310502D]
[5]
Collins, M.J., Jr Future trends in microwave synthesis. Future Med. Chem., 2010, 2(2), 151-155.
[http://dx.doi.org/10.4155/fmc.09.133] [PMID: 21426181]
[6]
Ravichandran, S.; Karthikeyan, E. Microwave Synthesis - A Potential Tool for Green Chemistry. Int. J. Chemtech Res., 2011, 3(1), 466-470.
[7]
G, B.R.; Dadigala, R.; Bandi, R.; Seku, K.; D, K.; Mangatayaru K, G.; Shalan, A.E. Microwave-assisted preparation of a silver nanoparticles/N-doped carbon dots nanocomposite and its application for catalytic reduction of rhodamine B, methyl red and 4-nitrophenol dyes. RSC Advances, 2021, 11(9), 5139-5148.
[http://dx.doi.org/10.1039/D0RA10679H] [PMID: 35424440]
[8]
Hashtroudi, H.; Kumar, R.; Savu, R.; Moshkalev, S.; Kawamura, G.; Matsuda, A.; Shafiei, M. Hydrogen gas sensing properties of microwave-assisted 2D Hybrid Pd/rGO: Effect of temperature, humidity and UV illumination. Int. J. Hydrogen Energy, 2021, 46(10), 7653-7665.
[http://dx.doi.org/10.1016/j.ijhydene.2020.11.268]
[9]
Chen, M.; He, Y.; Gu, Z. Microwave irradiation activated persulfate and hydrogen peroxide for the treatment of mature landfill leachate effluent from a membrane bioreactor. Separ. Purif. Tech., 2020, 250(3), 117111.
[http://dx.doi.org/10.1016/j.seppur.2020.117111]
[10]
Vasudevan, A. Microwave-Assisted Organic Synthesis - An Enabling Technology with Disruptive Potential. Drug Discov. World, 2008, 9(4), 83-90.
[11]
Mat Lazim, A.; Rohadi, A.; Hasbullah, S.A.; Mohamad, M.; Zul Ariff, A.L. Kaedah Gelombang Mikro: Alternatif Sintesis Sebatian Heterosiklik Konvensional. Sains Malays., 2021, 50(4), 1007-1016.
[http://dx.doi.org/10.17576/jsm-2021-5004-11]
[12]
Mavandadi, F.; Pilotti, Å. The impact of microwave-assisted organic synthesis in drug discovery. Drug Discov. Today, 2006, 11(3-4), 165-174.
[http://dx.doi.org/10.1016/S1359-6446(05)03695-0] [PMID: 16533715]
[13]
Kidwai, M.; Mothsra, P.; Bansal, V.; Somvanshi, R.K.; Ethayathulla, A.S.; Dey, S.; Singh, T.P. One-pot synthesis of highly substituted imidazoles using molecular iodine: A versatile catalyst. J. Mol. Catal. Chem., 2007, 265(1-2), 177-182.
[http://dx.doi.org/10.1016/j.molcata.2006.10.009]
[14]
Ren, Y.M.; Cai, C. A Solvent-Free Synthesis of 1,2,4,5-Tetrasubstituted Imidazoles Using Molecular Iodine as Catalyst. J. Chem. Res., 2010, 34(3), 133-134.
[http://dx.doi.org/10.3184/030823410X12659021476402]
[15]
Capello, C.; Fischer, U.; Hungerbühler, K. What is a green solvent? A comprehensive framework for the environmental assessment of solvents. Green Chem., 2007, 9(9), 927-993.
[http://dx.doi.org/10.1039/b617536h]
[16]
Rai, P.; Srivastava, M.; Singh, J.; Singh, J. Molecular iodine: a green and inclusive catalyst for the synthesis of highly functionalized 1,3,5-trisubstituted pyrazoles in aqueous medium. RSC Advances, 2014, 4(2), 779-783.
[http://dx.doi.org/10.1039/C3RA44315A]
[17]
Husain, A.; Drabu, S.; Kumar, N.; Alam, M.M.; Bawa, S. Synthesis and biological evaluation of di- and tri-substituted imidazoles as safer anti-inflammatory-antifungal agents. J. Pharm. Bioallied Sci., 2013, 5(2), 154-161.
[http://dx.doi.org/10.4103/0975-7406.111822] [PMID: 23833522]
[18]
Brahmbhatt, H.; Molnar, M.; Pavić, V. Pyrazole nucleus fused tri-substituted imidazole derivatives as antioxidant and antibacterial agents. Karbala Int. J. Modern Sci., 2018, 4(2), 200-206.
[http://dx.doi.org/10.1016/j.kijoms.2018.01.006]

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