Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 592268Generated: October 30, 2026

Sodium Thiosulfate → HCID 86646747, compound

https://huagongshe.com/reaction/592268

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactant2,6-Di-tert-butyl-4-methylphenolHCID 31404—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86646748HCID 86646748—
SolventChloroformHCID 6212—
ProductHCID 86646747HCID 86646747423.2%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of tert-butyl {(1R)-1-[6-(trifluoromethyl)-3-pyridinyl]ethyl}carbamate (0.626 g, 2.157 mmol) in chloroform (10.0 mL) were added 2,6-di-tert-butyl-4-methylphenol (24 mg, 0.108 mmol) and 3-chloroperbenzoic acid (0.665 g, 2.70 mmol). The reaction mixture was stirred at 50° C. for 48 h. The reaction mixture was cooled to ambient temperature. Saturated aqueous sodium thiosulfate and saturated aqueous sodium bicarbonate were added. The mixture was extracted with dichloromethane (3×). The combined organics extracts were washed with brine, dried over magnesium sulfate, filtered and concentrated. Purification by silica gel chromatography (75% hexanes/ethyl acetate 100% ethyl acetate) gave the title compound (140 mg). MS 307.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238647B2
Source datasetuspto-grants-2016_01
ORD IDord-613851f9af884716be27f1c42660b03d
Source noteuspto-grants-2016_01