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ChemicalBook CAS DataBase List Emodin
518-82-1

Emodin synthesis

11synthesis methods
-

Yield:518-82-1 98%

Reaction Conditions:

with boron tribromide in dichloromethane at 0 - 20;Inert atmosphere;

Steps:

General procedure of demethylation

To a solution of starting material (1 equiv) in dichloromethane (0.1 M) was added borontribromide (3.1 equiv per one methoxy group) at 0 °C. The reaction mixture was stirred at 0 °C,and warmed to room temperature for 1 h to overnight. After that, the reaction mixture was poured into ice water. The aqueous layer was extracted with dichloromethane three times. The combined organic layer was dried over anhydrous Na2SO4, filtered and concentrated. Thecrude product was purified by column chromatography to give desired demethylated product.

References:

Chalothorn, Thidarat;Rukachaisirikul, Vatcharin;Phongpaichit, Souwalak;Pannara, Sakawrat;Tansakul, Chittreeya [Tetrahedron Letters,2019,vol. 60,# 35,art. no. 151004] Location in patent:supporting information

Emodin Related Search:

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