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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1753674Generated: October 28, 2026

Hydrogen Peroxide → HCID 117666514, compound

https://huagongshe.com/reaction/1753674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantTolueneHCID 1140—
ReactantHCID 117666967HCID 117666967—
CatalystSodium Thiosulfate PentahydrateHCID 61475—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 117666514HCID 11766651499%

Reaction Steps

In 120 g of acetic acid was dissolved 17.1 g of phenyl 4-(2,2,2-trifluoroethoxy)phenyl sulfide obtained in Synthesis Example 1-13. While the solution was maintained at an internal temperature of 30° C., 5.8 g of 35 wt % aqueous hydrogen peroxide was added dropwise. The reaction solution was aged at room temperature for 18 hours, after which under ice cooling, a mixture of 0.5 g sodium thiosulfate pentahydrate and 15 g water was added dropwise to quench the reaction. The solution was combined with 100 g of toluene, 50 g of ethyl acetate, and 50 g of water. The organic layer was separated, washed with water, and concentrated in vacuum. This was followed by crystallization from hexane, filtration, and drying. There was obtained 17.9 g of the target compound, phenyl 4-(2,2,2-trifluoroethoxy)phenyl sulfoxide as white crystals. Yield 99%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09164384B2
Source datasetuspto-grants-2015_10
ORD IDord-e8fe73b89d354401a1f0fd14c968c7f4
Source noteuspto-grants-2015_10