HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426388Generated: October 31, 2026
Potassium Iodide → HCID 59561159, compound
https://huagongshe.com/reaction/426388
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Phosphinic Acid | HCID 4124402 | — |
| Reactant | HCID 59561152 | HCID 59561152 | — |
| Reactant | HCID 178418950 | HCID 178418950 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 59561159 | HCID 59561159 | 47.4% |
Reaction Steps
A solution of 46 mmol of 9,10-bis(9,9-dimethylfluorene-2-yl)-2-bromo-9,10-dihydroanthracene-9,10-diol, 24 g (0.23 mol) of sodium phosphinate monohydrate, and 15 g (91 mmol) of potassium iodide in 100 mL of glacial acetic acid was stirred for 4 hours at 120° C. After the reaction, 60 mL of a 50% phosphinic acid was added to the reaction mixture, and then stirring was kept for additional 2 hours at 120° C. Water was added to the mixture, and the mixture was stirred for 1 hour. After the mixture was filtered, the resulting solid was washed with water and dissolved in toluene, and the toluene-solution was washed with a saturated sodium bicarbonate aqueous solution and brine. Magnesium sulfate was added to this organic layer to dry the organic layer. This mixture was subjected to suction filtration, and the filtrate was filtered through celite, Florisil, and then alumina. The filtrate was concentrated, and the resulting solid was dissolved in a mixed solvent of chloroform and methanol, which was followed by irradiating ultrasound to yield 14 g of the title compound as a light yellow solid. Total yield of the steps of (ii) and (iii) was 47%.
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-872257fe21ac4f8e8c2e1bf8c3adce75 |
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| Source note | uspto-grants-2012_01 |
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