Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791901Generated: November 3, 2026

Sodium Thiosulfate → 2-Chloro-5-(trifluoromethyl)pyridine 1-oxide

https://huagongshe.com/reaction/1791901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant2-Chloro-5-(trifluoromethyl)pyridineHCID 92342—
ReactantSodium BicarbonateHCID 516892—
SolventChloroformHCID 6212—
Product2-Chloro-5-(trifluoromethyl)pyridine 1-oxideHCID 1544834211.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

2-Chloro-5-trifluoromethylpyridine (5 g) was dissolved in chloroform (150 mL) and m-chloroperbenzoic acid (14.3 g) was added thereto. The mixture was stirred at 60° C. for 30 hr. Aqueous sodium thiosulfate solution and saturated aqueous sodium hydrogencarbonate solution were added to the reaction mixture, and after stirring, the mixture was extracted with chloroform. The extract was washed successively with saturated aqueous sodium hydrogencarbonate solution and brine, and dried. The solvent was evaporated under reduced pressure and the residue was purified by silica gel chromatography to give 2-chloro-5-trifluoromethylpyridine 1-oxide (0.64 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074794B2
Source datasetuspto-grants-2006_07
ORD IDord-d420f37c18ae4fd8aae271345f20a892
Source noteuspto-grants-2006_07