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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylsilyl iodide | HCID 85247 | — |
| Reactant | 3',4'-Bis(diethoxyphosphoryl)-[2,2':5',2'']-terthiophene | HCID 59155949 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3',4'-Diphosphono-[2,2';5',2'']-terthiophene | HCID 59155871 | 90% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08030438B2 |
|---|
| Source dataset | uspto-grants-2011_10 |
|---|
| ORD ID | ord-de29e2d7be804a69bc4f54071922c49b |
|---|
| Source note | uspto-grants-2011_10 |
|---|