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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161603Generated: October 25, 2026

Epothilone A → Epothilone C

https://huagongshe.com/reaction/1161603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpothilone AHCID 448799—
ReactantMagnesiumHCID 5462224—
CatalystHCID 178420582HCID 178420582—
SolventTetrahydrofuranHCID 8028—
ProductEpothilone CHCID 989122680%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a two-necked flask was added chopped pieces of magnesium turnings (24 mg, 1.0 mmol). The flask was flame-dried under vacuum and cooled under argon. Bis (cyclopentadienyl)titanium dichloride (250 mg, 1.0 mmol) was added followed by anhydrous THF (5 mL). The stirring suspension was evacuated with low vacuum, and the reaction flask was refilled with argon. The red suspension became dark, turning a homogeneous deep green after 1.5 h with nearly all the magnesium metal being consumed. An aliquot (3.5 mL, 0.70 mmol, 3.5 eq) was removed and cooled to −78° C. under argon. To this solution was added epothilone A (99 mg, 0.20 mmol, 1.0 eq). The reaction mixture was warmed to room temperature and stirred for 15 min. The volatiles were removed in vacuo and the residue was chromatographed two times on silica (25 g), eluting with 35% EtOAc/hexanes to give 76 mg (80%) of epothilone C as a pale yellow viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE041895E1
Source datasetuspto-grants-2010_10
ORD IDord-fde89054fa974363a2bde3d7807b5c09
Source noteuspto-grants-2010_10