HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537594Generated: October 26, 2026
Potassium Carbonate → 9-(4-Bromophenyl)-10-phenylanthracene
https://huagongshe.com/reaction/537594
Participants
| Role | Name | HCID | Charge |
|---|
| 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 | 45% |
Reaction Steps
A mixture of 1.0 g (2.63 mmol) of 9-iodo-10-phenylanthracene, 542 mg (2.70 mmol) of p-bromo phenylboronic acid, 46 mg (0.03 mmol) of tetrakis(triphenylphosphine)palladium(0) (abbreviation: Pd(PPh3)4), 3 mL (6 mmol) of potassium carbonate aqueous solution (2 mol/L), and 10 mL of toluene was stirred for nine hours at 80° C. After reaction, toluene was added and filtration was carried out using florisil, celite, and alumina. A filtrate was washed with water and saturated saline, and then dried with magnesium sulfate. After the mixture was subjected to natural filtration, the filtrate was concentrated, and when it was recrystallized with chloroform and hexane, 562 mg of 9-phenyl-10-(4-bromophenyl)anthracene that was a target substance is obtained as a light brown solid at a yield of 45% (Synthesis scheme (b-4)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08860019B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-9a9cdcc7ac1d4957a7846bbe89bb3a07 |
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| Source note | uspto-grants-2014_10 |
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