HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460448Generated: October 29, 2026
Water → 6-Methoxy-2-(4-methoxyphenyl)-1-(2-propenyl)naphthalene
https://huagongshe.com/reaction/460448
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | (4-Methoxyphenyl)boronic acid | HCID 201262 | — |
| Reactant | 6-Methoxy-1-(2-propenyl)-2-naphthyl trifluoromethanesulfonate | HCID 20726847 | — |
| Reactant | Potassium phosphate, tribasic, monohydrate | HCID 22031701 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 6-Methoxy-2-(4-methoxyphenyl)-1-(2-propenyl)naphthalene | HCID 22718010 | 75% |
Reaction Steps
4-Methoxyphenylboronic acid (10.15 g, 66.8 mmol), tripotassium phosphate hydrate (77.6 g, 278.3 mmol) and tetrakis(triphenylphosphine)palladium(0)(1.93 g, 1.67 mmol, 3 mol %) were added to a solution of 6-methoxy-1-(2-propenyl)-2-naphthyl trifluoromethanesulfonate (19.3 g, 55.66 mmol) in dioxane (300 ml), followed by heating under reflux for 8 hours under argon atmosphere. Water was added to the reaction mixture, which was then extracted with ethyl acetate, washed with saturated aqueous sodium chloride, and dried over anhydrous sodium sulfate. After distilling off the solvent, the residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane=1/9), followed by recrystallization from hexane, to give 6-methoxy-2-(4-methoxyphenyl)-1-(2-propenyl)naphthalene (12.65 g, Yield 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07196081B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-0f9820b897124778ac8efa1f1005aa6f |
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| Source note | uspto-grants-2007_03 |
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