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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773060Generated: October 26, 2026

Cesium carbonate → 4,6-Diphenyl-2-[3-(1,10-phenanthrolin-2-yl)phenyl]-1,3,5-triazine

https://huagongshe.com/reaction/1773060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantTriphenylphosphineHCID 11776—
Reactant2-(3-Bromophenyl)-4,6-diphenyl-1,3,5-triazineHCID 58943302—
Reactant2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1,10-phenanthrolineHCID 90401507—
Catalystpalladium(II) acetateHCID 167845—
SolventTetrahydrofuranHCID 8028—
Product4,6-Diphenyl-2-[3-(1,10-phenanthrolin-2-yl)phenyl]-1,3,5-triazineHCID 90401574—

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-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-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, and the deposited solid was collected by filtration. The thus-obtained crude product was 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 4,6-diphenyl-2-[3-(1,10-phenanthrolin-2-yl)phenyl]-1,3,5-triazine as a white solid (yield, 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09252368B2
Source datasetuspto-grants-2016_02
ORD IDord-eaf9331c2d51414f8a6e7c79b44aa520
Source noteuspto-grants-2016_02