Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639483Generated: November 3, 2026

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

https://huagongshe.com/reaction/1639483

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%

Reaction Conditions

Temperature80 °C

Reaction Steps

Into a 50 mL three-neck flask were put 1.0 g (2.63 mmol) of 9-iodo-10-phenylanthracene and 542 mg (2.70 mmol) of p-bromophenyl boronic acid. The atmosphere in the flask was replaced with nitrogen. After that, 10 mL of toluene and 3 mL of potassium carbonate aqueous solution (2.0 M) were added to the flask. This mixture was degassed under reduced pressure, then 46 mg (0.03 mmol) of tetrakis(triphenylphosphine)palladium(0) was added to the mixture. The mixture was stirred under a nitrogen stream at 80° C. for 9 hours. After the stirring, about 20 mL of toluene was added to this mixture. Then, the mixture was subjected to suction filtration through Florisil (produced by Wako Pure Chemical Industries, Ltd., Catalog No. 540-00135), Celite (produced by Wako Pure Chemical Industries, Ltd., Catalog No. 531-16855), and alumina. The obtained filtrate was washed with water and a saturated saline, and then dried with magnesium sulfate. This mixture was gravity filtered, and the obtained filtrate was concentrated to give a solid. The obtained solid was recrystallized with chloroform/hexane to give 0.56 g of a light-brown solid, which was the object of the synthesis, in a yield of 45%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110122B2
Source datasetuspto-grants-2012_02
ORD IDord-e5b9ffe24bfb4755865481d8a016576f
Source noteuspto-grants-2012_02