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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773062Generated: October 26, 2026

Cesium carbonate → 2-[4'-(1,10-Phenanthrolin-2-yl) biphenyl-3-yl]-4,6-diphenyl-1,3,5-triazine

https://huagongshe.com/reaction/1773062

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantTriphenylphosphineHCID 11776—
Reactant2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1,10-phenanthrolineHCID 58340445—
Reactant2-(3-Bromophenyl)-4,6-diphenyl-1,3,5-triazineHCID 58943302—
Catalystpalladium(II) acetateHCID 167845—
SolventTetrahydrofuranHCID 8028—
Product2-[4'-(1,10-Phenanthrolin-2-yl) biphenyl-3-yl]-4,6-diphenyl-1,3,5-triazineHCID 90401645—

Reaction Steps

In a stream of argon, 1.20 g of 2-(3-bromophenyl)-4,6-diphenyl-1,3,5-triazine, 1.30 g of 2-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1,10-phenanthroline, 1.11 g of cesium carbonate, 14 mg of palladium acetate and 32 mg of triphenylphosphine were suspended in 140 mL of tetrahydrofuran. The suspension was heated under reflux for 19 hours. Then the reaction mixture was left to be cooled to room temperature, and distilled under a reduced pressure to remove low-boiling point ingredients. Methanol was added to the residue. The thus-deposited solid was collected by filtration, and purified by silica gel column chromatography using a methanol/chloroform (1:100 to 1:77) mixed solvent as a developing solvent to give 1.37 g of target 2-[4′-(1,10-phenanthrolin-2-yl) biphenyl-3-yl]-4,6-diphenyl-1,3,5-triazine as a white solid (yield, 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09252368B2
Source datasetuspto-grants-2016_02
ORD IDord-9ab4d87f8c144fe9853452a1cf7693f0
Source noteuspto-grants-2016_02