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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant2,4-Dichloro-5-(2,2,2-trifluoroethylthio)phenolHCID 117899748—
SolventChloroformHCID 6212—
Product2,4-Dichloro-5-(2,2,2-trifluoroethylsulfinyl)phenolHCID 11789968988%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09332754B2
Source datasetuspto-grants-2016_05
ORD IDord-a89b3c196e1d44bc8937ee2a5455e52a
Source noteuspto-grants-2016_05