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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369626Generated: November 1, 2026

Potassium Carbonate → 9-(4-Bromophenyl)-10-phenylanthracene

https://huagongshe.com/reaction/2369626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(4-Bromophenyl)boronic acidHCID 79599—
Reactant9-Iodo-10-phenylanthraceneHCID 14958373—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product9-(4-Bromophenyl)-10-phenylanthraceneHCID 2213827552.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

1.0 g (2.63 mmol) of 9-iodo-10-phenylanthracene, 542 mg (2.70 mmol) of p-bromophenylboronic acid, 46 mg (0.03 mmol) of tetrakis(triphenylphosphine)palladium(0) (Pd(PPh3)4), 3 mL (6 mmol) of an aqueous potassium carbonate (K2CO3) solution (2 mol/L), and 10 mL of toluene were collected, mixed, and stirred for 9 hours at 80° C. After the reaction, toluene was added and the mixture was filtered through florisil, Celite®, and alumina. The filtrate was washed with water and a saturated aqueous sodium chloride solution and then dried with magnesium sulfate. After natural filtration, the filtrate was concentrated and the obtained solid was recrystallized with chloroform and hexane, thereby obtaining 562 mg of objective 9-phenyl-10-(4-bromophenyl)anthracene as a light-brown solid with a yield of 45%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08704242B2
Source datasetuspto-grants-2014_04
ORD IDord-ec7029b0ebf44633a6336779a349cc16
Source noteuspto-grants-2014_04