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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2041983Generated: October 30, 2026

Sodium Thiosulfate → HCID 59577129, compound

https://huagongshe.com/reaction/2041983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 59577292HCID 59577292—
SolventDichloromethaneHCID 6344—
ProductHCID 59577129HCID 5957712990.5%

Reaction Steps

To an ice-cold stirred solution of (3-(2-tert-butylphenylthio)azetidin-1-yl)(phenyl)methanone (0.18 g, 0.55 mmol) in methylene chloride (10.0 mL) was added m-CPBA (0.15 g, 0.61 mmol). After 10 min a saturated solution of sodium thiosulfate and sodium hydrogen carbonate was added to the reaction mixture and the resulting reaction mixture was warmed to room temperature. After 30 min the reaction mixture was diluted with methylene chloride and separated. The organic layer was washed with saturated sodium chloride, dried (Na2SO4), filtered and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, 50:50 heptane/ethyl acetate) to provide (3-(2-tert-butylphenylsulfinyl)azetidin-1-yl)(phenyl)methanone (0.17 g, 66%) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586571B2
Source datasetuspto-grants-2013_11
ORD IDord-f50a4cf8870842c09f654181b6edf59d
Source noteuspto-grants-2013_11