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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700461Generated: October 30, 2026

5-(4-methoxyphenyl)cyclohexane-1,3-dione → HCID 18317344, compound

https://huagongshe.com/reaction/1700461

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(4-methoxyphenyl)cyclohexane-1,3-dioneHCID 347343—
ReactantSodium ethoxideHCID 2723922—
ReactantHCID 18317638HCID 18317638—
SolventEthanolHCID 702—
ProductHCID 18317344HCID 1831734412.5%

Reaction Steps

A mixture of 5-(4-methoxyphenyl)cyclohexane-1,3-dione (0.95 g), dimethyl-1,2-propadien-1-yl sulfonium bromide (1.5 g), sodium ethoxide (0.31 g) and ethanol (10 ml) was refluxed for 5 hours. Under reduced pressure, the solvent was evaporated, and the residue was dissolved in ethyl acetate. The solution was washed with water and saturated brine, dried with magnesium sulfate and concentrated under reduced pressure. The residue was dissolved in toluene (20 ml), and to the solution was added p-toluenesulfonic acid(0.85 g). The mixture was stirred at room temperature for 1 hour. To the mixture was added ethyl acetate, and the mixture was washed with sodium hydrogen carbonate solution, water and saturated brine, dried with magnesium sulfate and concentrated under reduced pressure. The residue was purified with silica gel column chromatography (EtOAc/hexane) to give colorless crystals of 6-(4-methoxyphenyl)-3-methyl-4,5,6,7-tetrahydrobenzofuran-4-one (0.14 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06350749B1
Source datasetuspto-grants-2002_02
ORD IDord-a16b2ba41dde4b51884dc275e0aea271
Source noteuspto-grants-2002_02