HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075613Generated: October 29, 2026
Potassium Carbonate → 9-(4-Bromophenyl)-10-phenylanthracene
https://huagongshe.com/reaction/2075613
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
First, 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 a potassium carbonate (K2CO3) aqueous solution (2 mol/L), and 10 mL of toluene were mixed and stirred at 80° C. for nine hours. After the reaction, toluene was added therein, and the mixture was filtered through Florisil, Celite, and alumina. The filtrate was washed with water and saturated saline and then dried with magnesium sulfate. After the solution was filtered naturally, the filtrate was concentrated and recrystallized with chloroform and hexane; thus, 562 mg of a light-brown solid of 9-phenyl-10-(4-bromophenyl)anthracene as a target matter was obtained with a yield of 45%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07919773B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-55caa367fae5483db203f4854e9b82fa |
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| Source note | uspto-grants-2011_04 |
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