HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446658Generated: November 2, 2026
Potassium Iodide → HCID 59501382, compound
https://huagongshe.com/reaction/446658
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Phosphinic Acid | HCID 4124402 | — |
| Reactant | HCID 59501395 | HCID 59501395 | — |
| Reactant | HCID 178418950 | HCID 178418950 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 59501382 | HCID 59501382 | — |
Reaction Steps
In a recovery flask were placed 2-tert-butyl-9,10-bis[4-(5-phenyl-1,3,4-oxadiazol-2-yl)phenyl]anthracene-9,10-diol, 6.0 g (36 mmol) of potassium iodide, and 29 g (83 mmol) of sodium phosphinate monohydrate. They are dissolved by the addition of 50 mL of glacial acetic acid. This solution was stirred at 120° C. for 4 hours. Then, 50 mL of a 50% solution of phosphinic acid was added to this solution, and the mixture was stirred at 120° C. for 1 hour. Then, an aqueous solution of sodium hydrogen carbonate was added to this mixture, followed by stirring. After that, the resulting mixture was suction filtered to give a solid. This solid was washed with ethyl acetate. After that, the resulting solid was dissolved in chloroform, and this solution was washed with a saturated aqueous solution of sodium hydrogen carbonate and with saturated brine. Then, magnesium sulfate was added to the organic layer to thy it.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481176B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-ba608adbb08647dc828270301863ae70 |
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| Source note | uspto-grants-2013_07 |
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