Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Chloro-1,10-phenanthroline | HCID 355193 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | HCID 131734704 | HCID 131734704 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 131734703 | HCID 131734703 | — |
Reaction Steps
In a stream of argon, 1.13 g of 2-chloro-1,10-phenanthroline, 1.57 g of 2,4-di(3-biphenylyl-6-[3,5-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-phenyl]-1,3,5-triazine, 280 mg of lithium chloride and 203 mg of tetrakis(triphenylphosphine)palladium were suspended in a toluene (60 mL)/ethanol (15 mL) mixed solvent. 8.8 mL of a 2.0 M aqueous sodium carbonate solution was added in the obtained suspension, and the mixture was stirred at 100° C. for 65 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. The thus-obtained residue was purified by alumina column chromatography using chloroform as a developing solvent to give 1.22 g of target 2,4-di(3-biphenylyl-6-[3,5-bis(1,10-phenanthrolin-2-yl)phenyl]-1,3,5-triazine as a white powder (yield, 68%).
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-a647b43b884e43588fceaa35edfa4ea2 |
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| Source note | uspto-grants-2016_02 |
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