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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-(4-methoxyphenyl)cyclohexane-1,3-dione | HCID 347343 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | HCID 18317638 | HCID 18317638 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 18317344 | HCID 18317344 | 12.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06350749B1 |
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| Source dataset | uspto-grants-2002_02 |
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| ORD ID | ord-a16b2ba41dde4b51884dc275e0aea271 |
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| Source note | uspto-grants-2002_02 |
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