ISSN

0974-4150 (Online)
0974-4169 (Print)


Author(s): Nikunj Patadiya, Vipul Vaghela

Email(s): nikunj20899@gmail.com

DOI: 10.52711/0974-4150.2022.00036   

Address: Nikunj Patadiya1*, Vipul Vaghela2
1Research Scholar, Department of Pharmaceutical Chemistry, A.R College of Pharmacy and G.H Patel Institute of Pharmacy, Vallabh Vidhyanagar, Anand, Gujarat, India.
2Professor, Department of Pharmaceutical Chemistry, A.R College of Pharmacy and G.H Patel Institute of Pharmacy, Vallabh Vidhyanagar, Anand, Gujarat, India.
*Corresponding Author

Published In:   Volume - 15,      Issue - 3,     Year - 2022


ABSTRACT:
The main aim of present work is to develop optimised method for synthesis of 2’hydroxy chalcone. 2’hydroxy chalcone was synthesized by Claisen–Schmidt condensation between o-hydroxy acetohenone and benzaldehyde. Variety of bases tried as catalyst for synthesis of 2’hydroxy chalcone. Calcium hydroxide and magnesium hydroxide proved ineffective for synthesis. Lithium hydroxide slightly converts reactant to product. Sodium hydroxide shows best catalytical activity compare to other bases. Isopropyl alcohol proved better solvent then other solvents like methanol, ethanol, acetonitrile, dichloromethane and tetrahydrofuran. In optimization step, effect of solvent and base quantity, stirring time and temperature was examined. Temperature shows drastic effect on product yield and purity. At 0°C best yield was obtained. Amount of base catalyst also shows significant effect on yield. 20ml of 40% NaOH gives best results for 0.05mol reactants. 50ml IPA was needed for the best results for 0.05mol reactant. In approximate 4h, reaction should be completed. Further stirring was not too much effective.


Cite this article:
Nikunj Patadiya, Vipul Vaghela. An optimized method for synthesis of 2’hydroxy chalcone. Asian Journal of Research in Chemistry. 2022; 15(3):210-2. doi: 10.52711/0974-4150.2022.00036

Cite(Electronic):
Nikunj Patadiya, Vipul Vaghela. An optimized method for synthesis of 2’hydroxy chalcone. Asian Journal of Research in Chemistry. 2022; 15(3):210-2. doi: 10.52711/0974-4150.2022.00036   Available on: https://www.ajrconline.org/AbstractView.aspx?PID=2022-15-3-5


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