HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177819Generated: October 25, 2026
Potassium Iodide → 2-Bromo-9,10-diphenylanthracene
https://huagongshe.com/reaction/1177819
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Phosphinic Acid | HCID 4124402 | — |
| Reactant | 2-Bromo-9,10-diphenyl-9,10-dihydroanthracene-9,10-diol | HCID 23160218 | — |
| Reactant | HCID 178418950 | HCID 178418950 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-Bromo-9,10-diphenylanthracene | HCID 22247163 | 74% |
Reaction Steps
7.55 g (16.95 mmol) of the obtained 2-bromo-9,10-diphenyl-9,10-dihydroanthracene-9,10-diol, 5.06 g (30.51 mmol) of potassium iodide, 9.70 g (91.52 mmol) of sodium phosphinate monohydrate, and 50 mL of glacial acetic acid were put into a 500 mL three-neck flask, and the mixture was heated at 120° C. for 2 hours. Thereafter, 30 mL of 50% phosphinic acid was added to the mixture, and the mixture was stirred for 1 hour at 120° C. After the reaction, the mixture was washed with water, and the aqueous layer was extracted with ethyl acetate. The organic layer was dried over magnesium sulfate, filtered, and concentrated. The residue was dissolved in toluene, and the solution was filtered through celite, Florisil, and then alumina. The filtrate was concentrated, and the residue was recrystallized with chloroform and hexane, giving 5.1 g of 2-bromo-9,10-diphenylanthracene as a light yellow solid in 74% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07842945B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-44b959f434fc42579955fdecc8a3fd34 |
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| Source note | uspto-grants-2010_11 |
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