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ChemicalBook CAS DataBase List Coenzyme Q10
303-98-0

Coenzyme Q10 synthesis

9synthesis methods
-

Yield:303-98-0 100%

Reaction Conditions:

with iron(III) chloride in dichloromethane;acetonitrile at 0 - 5; for 0.5 h;Product distribution / selectivity;

Steps:

3; 8

Example 3 Oxidation of 2-hydroxy-3,4,5-trimethoxy-6-decaprenyl-toluene In a 100 ml flask 1.09 g (0.91 mmol) of 73.3% 2-hydroxy-3,4,5-trimethoxy-6-decaprenyl- toluene were dissolved in 4.1 ml of dichloromethane and 4.1 ml acetonitrile at 00C. To this solution 2.46 g FeCl3 ? 6 H2O (9.0 mmol, commercial from Riedel de Haen) in 8.2 ml of acetonitrile were added at 0-50C. After 30 minutes at 0-50C, 60 ml deionised water were added and the orange emulsion after addition of 60 ml 5% aqueous NaHCO3 solution was extracted with 250 ml of ether. The water layer was extracted with 60 ml of ether. The combined ether phases were dried over Na2SO4 and concentrated at 35°C under reduced pressure (20 to 10 mbar). The crude product (orange oil, 1.09 g, 100 %) was analysed by HPLC to be CoQlO; E/Z-ratio 95.8:4.2. The oxidation of the "trimethoxy-CoQIO" with FeCl3-OH2O to from CoQlO was effected as follows: EPO In a 100 ml flask 1.09 g of "trimethoxy-CoQlO" (0.91 mmol, 73.3 %) were dissolved in 4.1 ml of dichloromethane and 4.1 ml of acetonitrile at 0°C. To this solution 2.46 g of FeCl3 hexahydrate (9.0 mmol, commercial from Riedel de Haen) in 8.2 ml of acetonitrile were added at 0-50C. After half an hour at 0-5°C, 60 ml of deionised water were added and the orange emulsion after addition of 60 ml NaHCO3 solution (5%) was extracted with 250 ml of ether. The water layer was again extracted with 60 ml of ether. The combined ether phases were dried over Na2SO4 and concentrated at 35°C (20 -> 10 mbar). The crude product, CoQlO (orange oil, 1.09 g, 100 %), was analysed by HPLC. E/Z-ratio = 95.8:4.2.

References:

WO2007/17168,2007,A1 Location in patent:Page/Page column 9; 12-13

Coenzyme Q10 Related Search:

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