HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117827Generated: November 2, 2026
Potassium Carbonate → 9-(4-Bromophenyl)-10-phenylanthracene
https://huagongshe.com/reaction/2117827
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (4-Bromophenyl)boronic acid | HCID 79599 | — |
| Reactant | 9-Iodo-10-phenylanthracene | HCID 14958373 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 9-(4-Bromophenyl)-10-phenylanthracene | HCID 22138275 | 52.2% |
Reaction Steps
1.0 g (2.63 mmol) of 9-iodo-10-phenylanthracene, 542 mg (2.70 mmol) of p-bromophenylboronic acid, 46 mg (0.03 mmol) of tetrakis(triphenylphosphine)palladium(0) (Pd(PPh3)4), 3 mL (6 mmol) of an aqueous potassium carbonate (K2CO3) solution (2 mol/L), and 10 mL of toluene were collected, mixed, and stirred for 9 hours at 80° C. After the reaction, toluene was added and the mixture was filtered through florisil, Celite®, and alumina. The filtrate was washed with water and a saturated aqueous sodium chloride solution and then dried with magnesium sulfate. After natural filtration, the filtrate was concentrated and the obtained solid was recrystallized with chloroform and hexane, thereby obtaining 562 mg of objective 9-phenyl-10-(4-bromophenyl)anthracene as a light-brown solid with a yield of 45%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07442803B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-e0879bc65dad4a368bac4216e88ced14 |
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| Source note | uspto-grants-2008_10 |
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