Logo
International Journal of
Pharmaceutical Science and Research
ARCHIVES
VOL. 11, ISSUE 2 (2026)
Synthesis of 2-Amino-7-hydroxy-4-(4-methoxyphenyl)-4H-chromene-3-carbonitrile by using dealuminated mesolite as a heterogenous catalyst
Authors
Ahmad Lalahmad Shaikh
Abstract
In order to investigate optimum loading of catalyst and reaction condition, 4-OCH3 benzaldehyde (1mmol), resorcinol (1mmol), were reacted with malononitrile (1mmol) as model reaction with different amount of dealuminated mesolite as catalyst under reflux condition and results are summarized in (Table 1.1). In the absence of catalyst the reaction did not gave satisfactory yield of desired product (4c), which indicate crucial role of catalyst 0.1 g of dealuminated mesolite is suitable to catalyze reaction smoothly. The same reaction was carried out under different protic and aprotic solvents and it is observed that the reaction proceeds faster in protic solvent such as water and ethanol with maximum yield in reduced time as compare to non protic solvents such as terahydrofuran and actonitrile which gave lower yield.
Download
Pages:86-88
How to cite this article:
Ahmad Lalahmad Shaikh "Synthesis of 2-Amino-7-hydroxy-4-(4-methoxyphenyl)-4H-chromene-3-carbonitrile by using dealuminated mesolite as a heterogenous catalyst". International Journal of Pharmaceutical Science and Research, Vol 11, Issue 2, 2026, Pages 86-88

Please enter the email address corresponding to this article submission to download your certificate.

Synthesis of 2-Amino-7-hydroxy-4-(4-methoxyphenyl)-4H-chromene-3-carbonitrile by using dealuminated mesolite as a heterogenous catalyst | International Journal of Pharmaceutical Science and Research