HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662886Generated: October 29, 2026
Sodium Thiosulfate → 4,3'-Bis(diethoxyphosphoryl)-5'-iodo-[2,2']-bithiophene
https://huagongshe.com/reaction/1662886
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | 4,3'-Bis(diethoxyphosphoryl)-[2,2']-bithiophene | HCID 59155848 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4,3'-Bis(diethoxyphosphoryl)-5'-iodo-[2,2']-bithiophene | HCID 59155866 | 78% |
Reaction Steps
In a mixed solvent of chloroform and acetic acid at 1:1, 0.0877 g (0.2 mmols) of 4,3′-bis(diethoxyphosphoryl)-[2,2′]-bithiophene was dissolved, to which 0.2250 g (1.0 mmol) of commercially available N-iodosuccinimide was added at room temperature. Thereafter, the reaction mixture was stirred at room temperature for 8 hours. After the reaction, a sodium thiosulfate aqueous solution was added, followed by extraction with chloroform. The organic phase was washed with a 0.2 N sodium hydroxide aqueous 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 PTLC plate (developed with ethyl acetate:hexane=2:1) to obtain the specified substance in the form of a yellow solid at a yield of 0.0880 g (yield: 78%). The thus obtained product was used as it is for reaction in Example 12(12).
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-71c92725a88a48a79f8402022c9ea4f7 |
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| Source note | uspto-grants-2011_10 |
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