HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1190232Generated: October 25, 2026
Potassium Phosphate, Tribasic → 9-(4-Methylnaphth-1-yl)anthracene
https://huagongshe.com/reaction/1190232
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 9-Bromoanthracene | HCID 74062 | — |
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | 4-Methyl-1-naphthaleneboronic acid | HCID 2773511 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 9-(4-Methylnaphth-1-yl)anthracene | HCID 57702564 | — |
Reaction Steps
3.6 g (11.7 mmol) of tri-o-tolylphosphine and then 437 mg (1.9 mmol) of palladium(II) acetate are added with vigorous stirring to a suspension of 93.0 g (500 mmol) of 4-methylnaphthalene-1-boronic acid, 100.0 g (389 mmol) of 9-bromoanthracene, 212.3 g (1 mol) of tripotassium phosphate in a mixture of 400 ml of dioxane, 600 ml of toluene and 1000 ml of water, and the mixture is refluxed for 16 h. After the reaction mixture has been cooled, the organic phase is separated off and washed three times with 500 ml of water. The organic phase is subsequently filtered through silica gel and evaporated to dryness. The oil which remains is taken up in 1000 ml of ethanol and dissolved under reflux. After cooling, the colourless solid is filtered off with suction, again washed by stirring with 1000 ml of ethanol and finally dried under reduced pressure. Yield: 103.0 g (83.1% of theory), about 96% according to 1H-NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08674141B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-d3e7195fd1e04e5a961bd3f9a5a4a3f4 |
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| Source note | uspto-grants-2014_03 |
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