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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium FluorideHCID 522689—
Reactant2-(Tri-n-butylstannyl)thiopheneHCID 2779373—
Reactant2,5-Diiodo-3,4-bis(diethoxyphosphoryl)thiopheneHCID 86638411—
ReactantHCID 178418546HCID 178418546—
Product3,4-Bis(ethoxyphosphoryl)-[2,2']-bithiopheneHCID 86638410—

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030438B2
Source datasetuspto-grants-2011_10
ORD IDord-833783bcade544ad84eab1aee98fdc3c
Source noteuspto-grants-2011_10