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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2400239Generated: October 30, 2026

Potassium Phosphate, Tribasic → 9-(4-Methylnaphth-1-yl)-10-(4-trimethylsilyinaphthyl)anthracene

https://huagongshe.com/reaction/2400239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantTri-o-tolylphosphineHCID 80271—
Reactant9-(4-Methylnaphth-1-yl)anthraceneHCID 57702564—
Reactant4-Trimethylsilyinaphth-1-ylboronic acidHCID 59861196—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Solvent1,4-DioxaneHCID 31275—
Product9-(4-Methylnaphth-1-yl)-10-(4-trimethylsilyinaphthyl)anthraceneHCID 59861211—

Reaction Steps

1.78 g (5.6 mmol) of tri-o-tolylphosphine and 0.2 g (0.9 mmol) of palladium acetate are added to a vigorously stirred, degassed suspension of 22.8 g (93.3 mmol) of 4-trimethylsilyinaphth-1-ylboronic acid, 37.4 g (93.3 mmol) of 9-(4-methylnaphth-1-yl)anthracene and 90 g (230 mmol) of tripotassium phosphate in a mixture of 575 ml of water, 100 ml of dioxane and 860 ml of toluene, and the mixture is refluxed for 60 h. After cooling, the organic phase is separated off, washed three times with 200 ml of water and once with 200 ml of saturated aqueous sodium chloride solution and subsequently dried over magnesium sulfate. After the desiccant has been filtered off, the organic phase is evaporated to dryness under reduced pressure in a rotary evaporator. The grey residue obtained in this way is recrystallised from dioxane. The deposited crystals are filtered off with suction, washed with 50 ml of ethanol and subsequently dried under reduced pressure; yield: 38 g, 79% of theory; purity: 99.9% according to HPLC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08795847B2
Source datasetuspto-grants-2014_08
ORD IDord-b563cb31190f4d76bd2fd008dd292eda
Source noteuspto-grants-2014_08