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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-(3-Bromophenyl)-4,6-diphenyl-1,3,5-triazine | HCID 58943302 | — |
| Reactant | 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1,10-phenanthroline | HCID 90401507 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4,6-Diphenyl-2-[3-(1,10-phenanthrolin-2-yl)phenyl]-1,3,5-triazine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09252368B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-eaf9331c2d51414f8a6e7c79b44aa520 |
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| Source note | uspto-grants-2016_02 |
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