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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662878Generated: October 30, 2026

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

https://huagongshe.com/reaction/1662878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
Reactant3'',4''-Bis(diethoxyphosphoryl)-[2,2';5',2'';5'',2''';5''',2'''']-quinquethiopheneHCID 59155924—
SolventAcetonitrileHCID 6342—
Product3'',4''-Diphosphono-[2,2';5',2'';5'',2''';5''',2'''']-quinquethiopheneHCID 5915587671%

Reaction Steps

In 4.0 ml of acetonitrile, 0.2746 g (0.401 mmols) of 3″,4″-bis(diethoxyphosphoryl)-[2,2′;5′,2″;5″,2″′;5″′,2″″]-quinquethiophene was dissolved, to which 0.4012 g (2.005 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. A sodium thiosulfate aqueous solution was added, followed by stirring, filtration of the precipitated crystals, washing with distilled water, methanol, chloroform and diethyl ether and drying to obtain the specified substance in the form of a yellow powder at a yield of 0.1630 g (yield: 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030438B2
Source datasetuspto-grants-2011_10
ORD IDord-b05147d46ffb4d2ba5172cda13223006
Source noteuspto-grants-2011_10