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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075613Generated: October 29, 2026

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

https://huagongshe.com/reaction/2075613

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

First, 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 a potassium carbonate (K2CO3) aqueous solution (2 mol/L), and 10 mL of toluene were mixed and stirred at 80° C. for nine hours. After the reaction, toluene was added therein, and the mixture was filtered through Florisil, Celite, and alumina. The filtrate was washed with water and saturated saline and then dried with magnesium sulfate. After the solution was filtered naturally, the filtrate was concentrated and recrystallized with chloroform and hexane; thus, 562 mg of a light-brown solid of 9-phenyl-10-(4-bromophenyl)anthracene as a target matter was obtained with a yield of 45%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919773B2
Source datasetuspto-grants-2011_04
ORD IDord-55caa367fae5483db203f4854e9b82fa
Source noteuspto-grants-2011_04