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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662873Generated: October 29, 2026

Potassium Fluoride → HCID 59155917, compound

https://huagongshe.com/reaction/1662873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium FluorideHCID 522689—
ReactantHCID 59155829HCID 59155829—
ReactantHCID 59155960HCID 59155960—
CatalystCuprous chlorideHCID 62652—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59155917HCID 5915591777%

Reaction Steps

In THF, 0.155 g (0.201 mmols) of the 5,5″-diiodo-3′,4′-bis(diethoxyphosphoryl)-[2,2′;5′,2″]-terthiophene obtained in Example 7(4) and 0.307 g (0.422 mmols) of 5-tributylstannyl-3,4-bis(diethoxyphosphoryl)-[2,2′]-bithiophene obtained in Example 6(5) were dissolved, to which 0.0438 g (0.442 mmols) of commercially available copper(I) chloride was added at room temperature. Thereafter, the reaction mixture was heated and stirred under reflux for 18 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. Subsequently, 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 crude product was purified with a silica gel column to obtain the specified substance in the form of a yellow oil at a yield of 0.216 g (yield: 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030438B2
Source datasetuspto-grants-2011_10
ORD IDord-f019d0f764ca413fb948f41ae347aeb1
Source noteuspto-grants-2011_10