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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | 3'',4''-Bis(diethoxyphosphoryl)-[2,2';5',2'';5'',2''';5''',2'''']-quinquethiophene | HCID 59155924 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3'',4''-Diphosphono-[2,2';5',2'';5'',2''';5''',2'''']-quinquethiophene | HCID 59155876 | 71% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08030438B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-b05147d46ffb4d2ba5172cda13223006 |
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| Source note | uspto-grants-2011_10 |
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