HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426381Generated: October 30, 2026
Potassium Iodide → HCID 20771554, compound
https://huagongshe.com/reaction/426381
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Phosphinic Acid | HCID 4124402 | — |
| Reactant | HCID 20771553 | HCID 20771553 | — |
| Reactant | HCID 178418950 | HCID 178418950 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 20771554 | HCID 20771554 | 66.2% |
Reaction Steps
18.32 g (30.66 mmol) of the obtained 9,10-di(2-biphenylyl)-2-bromo-9,10-dihydroanthracene-9,10-diol, 9.16 g (55.19 mmol) of potassium iodide, 17.55 g (165.56 mmol) of sodium phosphinate monohydrate, and 150 mL of glacial acetic acid were put into a three-neck flask, and the mixture was stirred for 5 hours at 120° C. Thereafter, 100 mL of 50% phosphinic acid was added to the mixture, followed by stirring for 1 hour at 120° C. After the reaction, the solution was washed with water, and the precipitate was filtered, recrystallized with chloroform and hexane, obtaining 11.4 g of 9,10-di(2-biphenylyl)-2-bromoanthracene as a light yellow solid in 66% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08106392B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-353c00f8bc3344729a9e1ab990a01317 |
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| Source note | uspto-grants-2012_01 |
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