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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2955Generated: October 28, 2026

Ethyl Acetate → HCID 18936412, compound

https://huagongshe.com/reaction/2955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantMagnesiumHCID 5462224—
Reactant5-[[3-(1,1-Dimethylethyl)-4-hydroxyphenyl]methylene]-4-thiazolidinoneHCID 54468549—
SolventMethanolHCID 887—
ProductHCID 18936412HCID 1893641272.9%

Reaction Steps

A portion of the title compound from Example 77 (395.1 mg; 1.5 mmol) was dissolved in 9 ml of methanol. Magnesium (72.9 mg; 3.0 mmol) was then added to the solution and the resulting reaction mixture was stirred at room temperature for 3 hours. After 3 hours, most of the magnesium which had been added originally appeared to be gone so an additional 182.3 mg (7.5 mmol) of magnesium were added. Stirring of the reaction solution at room temperature continued overnight. By the next morning a yellow precipitate had formed. This precipitate was dissolved by adding the methanolic reaction solution to an ethyl acetate/1N hydrochloric acid mixture. The organic layer from the resulting two-phase mixture was isolated and then dried over sodium sulfate. The volatile components of the organic layer were removed and the resulting residue was chased with methylene chloride. The residue was then dissolved in 25 ml of methylene chloride and the resulting solution was chromatographed on a silica gel chromatography column using a 5-20% isopropyl alcohol in hexanes gradient. Those fractions identified as containing essentially pure product were evaporated to provide 0.29 g of title compound. m.p. 65°-70° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05731336
Source datasetuspto-grants-1998_03
ORD IDord-da305453c99c4c2c9addcfb5438c3fa0
Source noteuspto-grants-1998_03