HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662865Generated: October 29, 2026
Potassium Fluoride → HCID 86638406, compound
https://huagongshe.com/reaction/1662865
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | 2-(Tri-n-butylstannyl)thiophene | HCID 2779373 | — |
| Reactant | HCID 86638408 | HCID 86638408 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86638406 | HCID 86638406 | — |
Reaction Steps
3,4-bis(diethoxyphosphoryl)-2-iodothiophene, different types of palladium catalysts (0.05 equivalents, commercially available products) indicated in the following Table 5 and commercially available copper(I) cyanide (0.20 equivalents) were dissolved in toluene, to which 2-tributylstannylthiophene (1.2 equivalents) was added at room temperature. Thereafter, the reaction mixture was heated to 70° C. and stirred for 8.5 to 10 hours. After the reaction, the reaction mixture was cooled down to room temperature, to which a potassium fluoride aqueous solution was added, followed by stirring for 2 hours. The resulting solid was removed by celite filtration and the filtrate was extracted with ethyl acetate. The organic phase was washed with a saturated saline solution and dried over anhydrous sodium sulfate. The solvent was removed by distilling off under reduced pressure, and the resulting crude product was purified with a silica gel column (ethyl acetate:methanol=15:1) to obtain the specified substances.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08030438B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-893e356f0929465999506dc54dd742e0 |
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| Source note | uspto-grants-2011_10 |
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