HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773063Generated: November 1, 2026
Potassium Carbonate → HCID 89568606, compound
https://huagongshe.com/reaction/1773063
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl | HCID 11155794 | — |
| Reactant | HCID 71039292 | HCID 71039292 | — |
| Reactant | HCID 89568605 | HCID 89568605 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 89568606 | HCID 89568606 | — |
Reaction Steps
In a stream of argon, 517 mg (0.996 mmol) of 2-[5-(anthracen-9-yl)-3-chlorophenyl]-4,6-diphenylpyrimidine, 299 mg (1.20 mmol) of 4-(quinolin-2-yl)phenylboronic acid and 4.5 mg (20 μmol) of palladium acetate and 29.6 mg (60 μmol) of 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl were suspended in a toluene (4.5 mL)/n-butanol (0.5 mL) mixed solvent, and the suspension was heated to 95° C. 800 μL (2.40 mmol) of an aqueous 3.0M potassium carbonate solution was gradually dropwise added to the mixture, and the mixture was stirred at that temperature for 2 hours. Then the reaction mixture was left to be cooled to room temperature, and water was added to the reaction mixture. Then the deposited solid was collected by filtration to give 645 mg of target 2-[5-(anthracen-9-yl)-4′-(quinoline-2-yl) biphenyl-3-yl]-4,6-diphenylpyrimidine as a white solid (yield, 94%).
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-4874cf75710c4b4baa5d767d06eba6e6 |
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| Source note | uspto-grants-2016_02 |
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