HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522450Generated: October 30, 2026
Sodium Thiosulfate → 2,4-Dichloro-5-(2,2,2-trifluoroethylsulfinyl)phenol
https://huagongshe.com/reaction/522450
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 2,4-Dichloro-5-(2,2,2-trifluoroethylthio)phenol | HCID 117899748 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2,4-Dichloro-5-(2,2,2-trifluoroethylsulfinyl)phenol | HCID 117899689 | 88% |
Reaction Steps
In 80 ml of chloroform was dissolved 10.0 g (36.08 mmol) of 2,4-dichloro-5-(2,2,2-trifluoroethylthio)phenol. Thereto was added 9.80 g (39.75 mmol) of 3-chloroperbenzoic acid (purity: about 70%) under ice cooling, and the mixture was stirred for 30 minutes at room temperature. Then, saturated aqueous solution of sodium thiosulfate was added to the reaction mixture to decompose excess peroxide. Thereafter, the solvent was distilled off under reduced pressure, and extraction was conducted by adding ethyl acetate and water. The organic phase obtained was washed by aqueous potassium carbonate solution and saturated aqueous sodium chloride solution in this order, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, to obtain 9.30 g (yield: 88%) of an intended product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09332754B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-a89b3c196e1d44bc8937ee2a5455e52a |
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| Source note | uspto-grants-2016_05 |
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