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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662885Generated: October 29, 2026

Potassium Fluoride → 4,3'-Bis(diethoxyphosphoryl)-[2,2']-bithiophene

https://huagongshe.com/reaction/1662885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium FluorideHCID 522689—
ReactantHCID 59155826HCID 59155826—
ReactantHCID 59155833HCID 59155833—
CatalystCuprous chlorideHCID 62652—
SolventTolueneHCID 1140—
Product4,3'-Bis(diethoxyphosphoryl)-[2,2']-bithiopheneHCID 5915584884%

Reaction Steps

At room temperature, 1.4875 g (4.3 mmols) of 5-iodo-3-(diethoxyphosphoryl)thiophene and 0.0994 g (0.086 mmols) of commercially available tetrakistriphenylphosphine palladium were dissolved in 43 ml of toluene, to which 2.1899 g (4.3 mmols) of 2-tributylstannyl-3-(diethoxyphosphoryl)thiophene and 0.0347 g (0.39 mmols) of commercially available copper(I) chloride were added at room temperature. Thereafter, the reaction mixture was heated and stirred under reflux for 3.5 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 1 hour. Thereafter, the solid was removed by celite filtration and the filtrate was extracted with ethyl acetate. The resulting 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 (gradiated with acetone from ethyl acetate) to obtain the specified substance in the form of a yellow oil at a yield of 1.5836 g (yield: 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030438B2
Source datasetuspto-grants-2011_10
ORD IDord-51a2383e42a741d4b7d7d4b6de79f52d
Source noteuspto-grants-2011_10