HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2361200Generated: October 31, 2026
Potassium Carbonate → 9-(4-Bromophenyl)-10-phenylanthracene
https://huagongshe.com/reaction/2361200
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 | — |
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 (abbreviation: Pd(PPh3)4 ), 3 mL (6 mmol) of potassium carbonate solution (2 mol/L), and 10 mL of toluene was stirred for 9 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 a mixed solution was naturally filtered and a filtrate was concentrated, an obtained solid was recrystallized with a mixture of chloroform and hexane. Then, 562 mg of 9-phenyl-10-(4-bromophenyl)anthracene (PA) that was a target substance and was a light brown solid was obtained in a yield of 45% (Synthesis Scheme (b-4)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08686628B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-5ec7bd71b6014c688fe4029882d3fa7c |
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| Source note | uspto-grants-2014_04 |
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