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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2273495Generated: October 30, 2026

Potassium Carbonate → 4,6-Diphenyl-2-[5-(9-phenanthryl)-3'-(3-pyridyl)biphenyl-3-yl]-1,3,5-triazine

https://huagongshe.com/reaction/2273495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant9-Phenanthracenylboronic acidHCID 11775704—
Reactant2-(3,5-Dibromophenyl)-4,6-diphenyl-1,3,5-triazineHCID 58382615—
Reactant(3-(Pyridin-3-yl)phenyl)boronic acidHCID 58526507—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
Product4,6-Diphenyl-2-[5-(9-phenanthryl)-3'-(3-pyridyl)biphenyl-3-yl]-1,3,5-triazineHCID 8666995342%

Reaction Steps

In a stream of argon, 0.71 g (3.21 mmol) of 9-phenanthreneboronic acid, 1.50 g (3.21 mmol) of 2-(3,5-dibromophenyl)-4,6-diphenyl-1,3,5-triazine and 37.0 mg (0.0321 mmol) of tetrakis(triphenylphosphine)palladium were suspended in a mixed solvent composed of 120 mL of toluene and 15 mL of ethanol, and the resultant suspension was heated to 60° C. To the suspension, 9.63 mL (9.63 mmol) of an aqueous 1M K2CO3 solution was gradually added dropwise, and the mixture was stirred for 8 hours. Then the mixture was cooled to room temperature, and 0.59 g (4.82 mmol) of 3-(3-pyridyl)phenylboronic acid and 9.63 mL (9.63 mmol) of an aqueous 1M K2CO3 solution were added. Then the mixture was heated to 60° C. and maintained at that temperature for 18 hours while being stirred. Then the reaction mixture was cooled to room temperature, and was then distilled under a reduced pressure to remove all volatile materials. Methanol was added to the concentrate, and the thus-deposited solid was collected by filtration. The obtained crude product was purified by silica gel chromatography using a hexane/chloroform (1:2) mixed solvent as an eluent to give 0.86 g of the target 4,6-diphenyl-2-[5-(9-phenanthryl)-3′-(3-pyridyl)biphenyl-3-yl]-1,3,5-triazine as a white solid (yield: 42%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120773B2
Source datasetuspto-grants-2015_09
ORD IDord-a278b082335648f698dec51cb4564cdc
Source noteuspto-grants-2015_09