Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantN-IodosuccinimideHCID 120273—
Reactant4,3'-Bis(diethoxyphosphoryl)-[2,2']-bithiopheneHCID 59155848—
SolventAcetic AcidHCID 176—
SolventChloroformHCID 6212—
Product4,3'-Bis(diethoxyphosphoryl)-5'-iodo-[2,2']-bithiopheneHCID 5915586678%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030438B2
Source datasetuspto-grants-2011_10
ORD IDord-71c92725a88a48a79f8402022c9ea4f7
Source noteuspto-grants-2011_10