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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1587240Generated: October 26, 2026

Water → 7-O-(Triethylsilyl)-10-deacetyl Baccatin III

https://huagongshe.com/reaction/1587240

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantChlorotriethylsilaneHCID 13819—
Reactant10-deacetylbaccatin IIIHCID 154272—
SolventPyridineHCID 1049—
Product7-O-(Triethylsilyl)-10-deacetyl Baccatin IIIHCID 1173498278%

Reaction Conditions

Temperature0 °C

Reaction Steps

544 mg (1 mmol) of 10-deacetylbaccatine III, dissolved in 50 cm3 of anhydrous pyridine, are introduced under an argon atmosphere into a 100-cm3 round-bottomed flask equipped with a magnetic stirrer. 3.36 cm3 (3.014 g; 20 mmol) of triethylsilyl chloride are then added. The homogeneous, yellow reaction mixture is then stirred for 24 hours at 0° C. Ethyl acetate and water are then added. After settling has taken place, the separated aqueous phase is extracted with ethyl acetate. The combined organic phases are treated with saturated aqueous copper sulphate solution until the pyridine has been completely removed. The organic phases are washed with water and then with saturated sodium chloride solution, and then dried over anhydrous sodium sulphate. After filtration and evaporation of the solvents under reduced pressure, 2.73 g of a product are obtained, and this is purified on a silica column, eluting with a dichloromethane/methanol (99:1 by volume) mixture. 512 mg (0.778 mmol) of 10-deacetyl-7-triethylsilylbaccatine III are thereby obtained, in a 78% yield, in the form of a white solid, the characteristics of which are as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE034277
Source datasetuspto-grants-1993_06
ORD IDord-7f9a7c8d6c7049fcbf94c4d22af5457d
Source noteuspto-grants-1993_06