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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant9-BromoanthraceneHCID 74062—
ReactantTri-o-tolylphosphineHCID 80271—
Reactant4-Methyl-1-naphthaleneboronic acidHCID 2773511—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Solvent1,4-DioxaneHCID 31275—
Product9-(4-Methylnaphth-1-yl)anthraceneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674141B2
Source datasetuspto-grants-2014_03
ORD IDord-d3e7195fd1e04e5a961bd3f9a5a4a3f4
Source noteuspto-grants-2014_03