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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662887Generated: October 29, 2026

Potassium Fluoride → 3,4',4''-Tri(diethoxyphosphoryl)-[2,2';5',2'']-terthiophene

https://huagongshe.com/reaction/1662887

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium FluorideHCID 522689—
ReactantHCID 59155833HCID 59155833—
Reactant4,3'-Bis(diethoxyphosphoryl)-5'-iodo-[2,2']-bithiopheneHCID 59155866—
ReactantHCID 178418546HCID 178418546—
SolventTolueneHCID 1140—
Product3,4',4''-Tri(diethoxyphosphoryl)-[2,2';5',2'']-terthiopheneHCID 5915589870%

Reaction Steps

At room temperature, 0.1129 g (0.2 mmols) of 4,3′-bis(diethoxyphosphoryl)-5′-iodo-[2,2′]-bithiophene and 0.0092 g (0.008 mmols) of commercially available tetrakistriphenylphosphine palladium were dissolved in 2 ml of toluene, to which 0.1018 g (0.2 mmols) of 2-(tributylstannyl)-3-(diethoxyphosphoryl)thiophene and 0.0036 g (0.04 mmols) of commercially available copper(I) cyanide were added at room temperature. Thereafter, the reaction mixture was heated and stirred under reflux for 2.5 hours. After the reaction, the reaction mixture was cooled down to room temperature, to which a potassium fluoride aqueous solution added, followed by stirring for 1 hour. 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 PTLC plate (developed with ethyl acetate:hexane=1:2 and ethyl acetate:hexane=1:1) to obtain the specified substance in the form of a yellow oil at a yield of 0.0919 g (yield: 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030438B2
Source datasetuspto-grants-2011_10
ORD IDord-ce0d56b2d4ad4e47901722c560466730
Source noteuspto-grants-2011_10