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chrysophanol dimethyl ether synthesis

12synthesis methods
-

Yield:71013-35-9 89%

Reaction Conditions:

with potassium carbonate in acetone; for 12 h;Reflux;

Steps:

4.2. General method for the preparation of ether derivatives ofnepodin and chrysophanol

General procedure: A conventional method of O-alkylation using potassium carbonate (K2CO3) as a base in aprotic solvent was used. To a stirred solution of 1 (0.69 mmol) containing potassium carbonate (1.17 mmol) in dry acetone (8e10 mL), an appropriate alkylating agent (1.04 mmol) was added dropwise and resulting reaction mixture was refluxed for 15-24 h. Progress of reaction was monitored by TLC. On completion, the reaction was quenched with water and aqueous portion was extracted with EtOAc (3 30 mL). Organic layer was passed over anhydrous Na2SO4 and solvent was removed under vacuum. The crude product was purified by CC (hexane/ethylacetate 98:2) to give desired 1- and 8-O-alkylated nepodin derivatives. Similar procedure was followed for the preparation of chrysophanol derivatives using 4 equiv of both potassium carbonate and alkylating agents.

References:

Grover, Jagdeep;Kumar, Vivek;Singh, Vikram;Bairwa, Khemraj;Sobhia, M. Elizabeth;Jachak, Sanjay M. [European Journal of Medicinal Chemistry,2014,vol. 80,p. 47 - 56]

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