HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640225Generated: November 1, 2026
Potassium Iodide → 2-Bromo-9,10-bis(4-fluorophenyl)anthracene
https://huagongshe.com/reaction/1640225
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Phosphinic Acid | HCID 4124402 | — |
| Reactant | 2-Bromo-9,10-bis(4-fluorophenyl)-9,10-dihydro-9,10-anthracenediol | HCID 59211150 | — |
| Reactant | HCID 178418950 | HCID 178418950 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-Bromo-9,10-bis(4-fluorophenyl)anthracene | HCID 59211105 | 74% |
Reaction Steps
8.32 (17.3 mmol) of 2-bromo-9,10-bis(4-fluorophenyl)-9,10-dihydro-9,10-anthracenediol, 5.17 g (31.1 mmol) of potassium iodide, 9.90 g (93.4 mmol) of sodium phosphinate monohydrate, and 50 mL of glacial acetic acid were put into a 200 mL three-neck flask, and the mixture was refluxed at 120° C. for 4 hours. Then, 20 mL of a 50% phosphinic acid was added into the reaction mixture, and the mixture was stirred for 1 hour at 120° C. After the reaction, the reaction mixture was washed with water, and the aqueous layer was extracted with ethyl acetate. This extracted solution was combined with the organic layer, and then dried with magnesium sulfate. After drying, the mixture was subjected to suction filtration, and the filtrate was concentrated. The obtained residue was dissolved in toluene, and filtered through Florisil, celite, and then alumina, and the filtrate was concentrated. The obtained residue was recrystallized with chloroform and hexane, giving 7.2 g of 2-bromo-9,10-bis(4-fluorophenyl)anthracene as light yellow powder in 74% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08110980B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-f68b97c1f4f9458bb5be0965f76fc71d |
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| Source note | uspto-grants-2012_02 |
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