Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 1-Naphthaleneboronic acid | HCID 254532 | — |
| Reactant | 2-[3-Chloro-5-(9-phenanthryl)phenyl]-4,6-diphenyl-1,3,5-triazine | HCID 86669966 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86669967 | HCID 86669967 | 95% |
Reaction Steps
Then in a stream of argon, 0.5 g (0.96 mmol) of the obtained 2-[3-chloro-5-(9-phenanthryl)phenyl]-4,6-diphenyl-1,3,5-triazine, 038 g (1.73 mmol) of 1-naphthaleneboronic acid, 12.9 mg (0.058 mmol) of palladium acetate and 1.13 g (3.46 mmol) of cesium carbonate were suspended in 50 mL of tetrahydrofuran, and the temperature of the obtained suspension was elevated to 70° C. and distilled under reflux for 40 hours. The resultant reaction mixture was cooled to room temperature, and 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 thus-obtained crude product was purified by column chromatography to give 0.56 g of the target 2-[3-(1-naphthyl)-5-(9-phenanthryl)phenyl]-4,6-diphenyl-1,3,5-triazine as grayish white solid (yield: 95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09120773B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-ea7122c2f7b34ed3b4dd6a5bc2499961 |
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| Source note | uspto-grants-2015_09 |
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