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OTAVA-BB BB7020402300 synthesis

5synthesis methods
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Yield:109386-28-9 79.2%

Reaction Conditions:

with sulfated montmorillonite K-10 in nitrobenzene at 100;Catalytic behavior;Green chemistry;

Steps:

General Procedure for the Synthesis of 4-Aryl-3,4-dihydrocoumarins 9-20

General procedure: A mixture of a substituted cinnamicacid (5 mmol) and a substituted phenol (5 mmol) in nitrobenzene (10 mL) was heated to 100C. Sulfated montmorilloniteK-10 (2 g) was added to the mixture after all reagents were dissolved, and the mixture was stirred at 100C for 3-12 h.The reaction process was monitored by TLC (CH2Cl2-CH3OH, 10:1). The suspension was directly filtered, and a suitableamount of petroleum ether was added to the filtrate. Then the mixture was cooled and stored or stirred under low temperaturefor a certain length of time to promote crystallization of the product. The crude product was recrystallized from EtOAc-PE toafford 9-20.

References:

Li, Na;Wang, Bing;Sun, Jing-yong;Wang, Xiao-jing;Sun, Jie [Chemistry of Natural Compounds,2017,vol. 53,# 5,p. 860 - 865][Khim. Prir. Soedin.,2017,vol. 53,# 5,p. 733 - 736,4]