HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662871Generated: October 29, 2026
Potassium Fluoride → 3,4-Bis(ethoxyphosphoryl)-[2,2']-bithiophene
https://huagongshe.com/reaction/1662871
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | 2-(Tri-n-butylstannyl)thiophene | HCID 2779373 | — |
| Reactant | 2,5-Diiodo-3,4-bis(diethoxyphosphoryl)thiophene | HCID 86638411 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Product | 3,4-Bis(ethoxyphosphoryl)-[2,2']-bithiophene | HCID 86638410 | — |
Reaction Steps
3,4-bis(diethoxyphosphoryl)-2,5-diiodothiophene obtained in Example 7, commercially available tetrakistriphenylphosphine palladium (0.10 equivalent) and copper(I) cyanide (commercial product) in amounts indicated in Table 8 were dissolved in different types of solvents indicated in Table 8, to which 2-tributylstannylthiophene (2.2 equivalents) was added at room temperature. Thereafter, the reaction mixture was heated to 70° C. and stirred for 6 to 20 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. Thereafter, the 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 product was purified with a silica gel column (ethyl acetate:methanol=15:1).
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-833783bcade544ad84eab1aee98fdc3c |
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| Source note | uspto-grants-2011_10 |
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