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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 626606Generated: October 30, 2026

Potassium Carbonate → 2-{3-[3-(Dibenzothiophen-4-yl)phenyl]phenyl}dibenzo[f,h]quinoline

https://huagongshe.com/reaction/626606

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTri-o-tolylphosphineHCID 80271—
Reactant(3-(Dibenzo[b,d]thiophen-4-yl)phenyl)boronic acidHCID 58261920—
Reactant2-(3-Bromophenyl)dibenzo[f,h]quinolineHCID 86675563—
Catalystpalladium(II) acetateHCID 167845—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product2-{3-[3-(Dibenzothiophen-4-yl)phenyl]phenyl}dibenzo[f,h]quinolineHCID 8667556263%

Reaction Steps

In a 50-mL three-neck flask, 0.56 g (1.5 mmol) of 2-(3-bromophenyl)dibenzo[f,h]quinoline, 0.46 g (1.5 mmol) of 3-(dibenzothiophen-4-yl)phenylboronic acid, 58 mg (0.19 mmol) of tri(ortho-tolyl)phosphine, 15 mL of toluene, 1.5 mL of ethanol, and 1.5 mL of a 2M aqueous solution of potassium carbonate were put. The mixture was degassed by being stirred under reduced pressure, and the air in the flask was replaced with nitrogen. Then, 17 mg (77 μmol) of palladium(II) acetate was added to this mixture, and the mixture was stirred at 80° C. for 9 hours under a nitrogen stream. After a predetermined time, water and toluene were added to this mixture, and the resulting solid was collected by suction filtration. A toluene solution of the obtained solid was suction-filtered through alumina and Celite, and the filtrate was concentrated to give a yellow solid. A methanol suspension of the obtained solid was irradiated with ultrasonic waves, and a solid was collected by suction filtration, so that the object of the synthesis was obtained as 0.52 g of white powder in 63% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309223B2
Source datasetuspto-grants-2016_04
ORD IDord-f9033963dc924b349ea16896d18172f4
Source noteuspto-grants-2016_04