Synthesis of Dihydrocoumarin derivatives from Methyl trans-Cinnamate And Evaluation of their Bioactivity as Potent anticancer Agents

Teni Ernawati, Harpolia Cartika, Muhammad Hanafi, Ms. Suzana, Dila Fairusi

Abstract


Synthesis of dihydrocoumarin derivatives from methyl trans-cinnamate is described. The reaction can be carried out as a simple one pot reaction using acid catalyst. Firstly, methyl trans-cinnamate was converted into cinnamic acid via hydrolysis reaction with alkaline. Secondly, esterification reaction of cinnamic acid was carried out by using an acid catalyst p-toluensulfonic acid with phenol, o-cresol, p-cresol which lead to the production of 4-phenylchroman-2-one, 8-methyl -4-phenylchroman-2-one, and 6-methyl-4-phenylchroman-2-one.

 

 


Keywords


dihydrocoumarin derivatives, methyl trans-cinnmate, cinnamic acid, 4-phenylchroman-2-one, 8-methyl -4- phenylchroman-2-one, and 6-methyl-4-phenylchroman-2-one

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