HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2361203Generated: October 25, 2026
Potassium Carbonate → 9-(4'-Bromobiphenyl-4-yl)-10-phenylanthracene
https://huagongshe.com/reaction/2361203
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4'-Bromo-4-biphenylboronic Acid (contains varying amounts of Anhydride) | HCID 3841607 | — |
| Reactant | 9-Iodo-10-phenylanthracene | HCID 14958373 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 9-(4'-Bromobiphenyl-4-yl)-10-phenylanthracene | HCID 58850660 | 45% |
Reaction Steps
1.0 g (2.63 mmol) of 9-iodo-10-phenylanthracene, 542 mg (2.70 mmol) of 4-(4-bromophenyl)phenylboronic acid, 46 mg (0.03 mmol) of tetrakis(triphenylphosphine)palladium, 3 mL (6 mmol) of potassium carbonate solution (2.0 mol/L), and 10 mL of toluene were stirred for 9 hours at 80° C. After reaction, toluene was added, and it was filtered through florisil®, celite, and alumina. The filtrate was washed with water and saturated saline, and then dried with magnesium sulfate. After natural filtering, the filtrate was concentrated, and when recrystallization was performed with a mixture of chloroform and hexane, 562 mg of 9-[4-(4-bromophenyl)phenyl]-10-phenylanthracene (PBA) that was a target substance and was a light brown solid was obtained in a yield of 45% (Synthesis Scheme (e-2)).
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-a211971aa32b4bf998cfa3026b7a5dd4 |
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| Source note | uspto-grants-2014_04 |
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