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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639481Generated: October 25, 2026

Sodium Carbonate → 9-(4'-Bromobiphenyl-4-yl)-10-phenylanthracene

https://huagongshe.com/reaction/1639481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4'-Bromo-4-biphenylboronic Acid (contains varying amounts of Anhydride)HCID 3841607—
Reactant9-Iodo-10-phenylanthraceneHCID 14958373—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product9-(4'-Bromobiphenyl-4-yl)-10-phenylanthraceneHCID 5885066040.1%

Reaction Steps

Into a 100 mL three-neck flask were put 2.8 g (7.2 mmol) of 9-iodo-10-phenylanthracene and 1.5 g (7.2 mmol) of 4′-bromobiphenyl-4-boronic acid, and the atmosphere in the flask was replaced with nitrogen. To the mixture, 40 mL of toluene and 10 mL (2.0 mol/L) of a sodium carbonate aqueous solution were added. The mixture was stirred under reduced pressure to be degassed. After the degassing, 120 mg (0.10 mmol) of tetrakis(triphenylphosphine)palladium(0) was added to the mixture. The mixture was stirred at 90° C. for 4 hours. After the stirring, about 50 mL of toluene was added to the mixture. The mixture was subjected to suction filtration through alumina, Celite (produced by Wako Pure Chemical Industries, Ltd., Catalog No. 531-16855), and Florisil (produced by Wako Pure Chemical Industries, Ltd., Catalog No. 540-00135). The solid obtained by condensation of the obtained filtrate was purified by high-performance liquid chromatography (the mobile phase: chloroform) to give a light yellow solid. The obtained solid was recrystallized with chloroform/hexane to give 1.4 g of a light yellow powdered solid, which was the object of the synthesis, in a yield of 40%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110122B2
Source datasetuspto-grants-2012_02
ORD IDord-0f333ae6ef194d888e520232a8012227
Source noteuspto-grants-2012_02