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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662877Generated: October 29, 2026

Trimethylsilyl iodide → 3',4'-Diphosphono-[2,2';5',2'']-terthiophene

https://huagongshe.com/reaction/1662877

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
Reactant3',4'-Bis(diethoxyphosphoryl)-[2,2':5',2'']-terthiopheneHCID 59155949—
SolventAcetonitrileHCID 6342—
Product3',4'-Diphosphono-[2,2';5',2'']-terthiopheneHCID 5915587190%

Reaction Steps

In acetonitrile, 0.2478 g (0.476 mmols) of 3′,4′-bis(diethoxyphosphoryl)-[2,2′;5′,2″]-terthiophene was dissolved, to which 0.4762 g (2.380 mmols) of commercially available iodotrimethylsilane was added at room temperature. Thereafter, the mixture was stirred at room temperature for 12 hours. After the reaction, the solvent was removed by distilling off under reduced pressure, followed by addition of methanol and stirring at room temperature for further 12 hours. The methanol was removed by distilling off under reduced pressure, followed by addition of distilled water under stirring and separation of an aqueous phase. The thus separated aqueous phase was washed several times with chloroform and the aqueous phase was concentrated and evaporated to dryness to obtain the specified substance in the form of yellow crystals at a yield of 0.1742 g (yield: 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030438B2
Source datasetuspto-grants-2011_10
ORD IDord-de29e2d7be804a69bc4f54071922c49b
Source noteuspto-grants-2011_10