2010Chemical ReagentsRequires access

Study on synthesis of 4-methyl-5,7-dihydroxylcoumarin catalyzed by amino-sulfonic acid under microwave irradiation

Xiaojun Yang

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Abstract

The synthesis of 4-methyl-5,7-dihydroxyl coumarin was performed via the condensation of 1,3,5-benzenetriol and ethyl acetoacetate under microwave irradiation.The optimum reaction conditions were as follows:6.7 g of 1,3,5-benzenetriol,6.8 mL of ethyl acetoacetate,0.1 g of aminosulfonic acid,10 mL of cyclohexane were subjected to reaction for 12 min at 100 ℃ under microwave irradiation with a microwave power of 380 W.The product yield reached 89.2%.

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What this paper is about

The synthesis of 4-methyl-5,7-dihydroxyl coumarin was performed via the condensation of 1,3,5-benzenetriol and ethyl acetoacetate under microwave irradiation.The optimum reaction conditions were as follows:6.7 g of 1,3,5-benzenetriol,6.8 mL of ethyl acetoacetate,0.1 g of aminosulfonic acid,10 mL of cyclohexane were subjected to reaction for 12 min at 100 ℃ under microwave irradiation with a microwave power of 380 W.The product yield reached 89.2%.

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Available abstract

The synthesis of 4-methyl-5,7-dihydroxyl coumarin was performed via the condensation of 1,3,5-benzenetriol and ethyl acetoacetate under microwave irradiation.The optimum reaction conditions were as follows:6.7 g of 1,3,5-benzenetriol,6.8 mL of ethyl acetoacetate,0.1 g of aminosulfonic acid,10 mL of cyclohexane were subjected to reaction for 12 min at 100 ℃ under microwave irradiation with a microwave power of 380 W.The product yield reached 89.2%.

Key concepts: Chemistry, Ethyl acetoacetate, Yield (engineering), Coumarin, Microwave irradiation, Catalysis, Sulfonic acid, Cyclohexane

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