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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658957Generated: October 30, 2026

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

https://huagongshe.com/reaction/658957

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 2213827545%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 1.0 g (2.63 mmol) of 9-iodo-10-phenylanthracene, 542 mg (2.70 mmol) of p-bromo phenylboronic acid, 46 mg (0.03 mmol) of tetrakis(triphenylphosphine)palladium(0) (abbreviation: Pd(PPh3)4), 3 mL (6 mmol) of potassium carbonate aqueous solution (2 mol/L), and 10 mL of toluene was stirred for nine hours at 80° C. After reaction, toluene was added and filtration was carried out using florisil, celite, and alumina. A filtrate was washed with water and saturated saline, and then dried with magnesium sulfate. After the mixture was subjected to natural filtration, the filtrate was concentrated, and when it was recrystallized with chloroform and hexane, 562 mg of 9-phenyl-10-(4-bromophenyl)anthracene that was a target substance is obtained as a light brown solid at a yield of 45% (Synthesis scheme (b-4)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08076676B2
Source datasetuspto-grants-2011_12
ORD IDord-5c8a0b25fef149d0ab4f9a205b353216
Source noteuspto-grants-2011_12