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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098756Generated: October 30, 2026

3'-(Trifluoromethylthio)acetophenone → HCID 59506285, compound

https://huagongshe.com/reaction/1098756

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3'-(Trifluoromethylthio)acetophenoneHCID 2777838—
ReactantPotassium hydroxy sulfiteHCID 23707502—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59506285HCID 5950628544%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 1-(3-trifluoromethylsulfanyl-phenyl)ethanone (1.4 g, 6.36 mmol) in methanol (30 ml) and THF (30 ml) a solution of oxone, monopersulfate compound (10.94 g, 17.8 mmol) in water (50 ml) was added dropwise over a period of 10 min. The reaction mixture was stirred at 60° C. for 3 days. The organic solvent was removed in vacuo and the aqueous phase was extracted with dichloromethane. Evaporation of the combined organic layers and purification of the crude product by silica gel chromatography using ethyl acetate/n-heptane gave the desired product (0.66 g, 44%). 1-(3-Trifluoromethanesulfonyl-phenyl)ethanone (190 mg, 12%) was obtained as a side product which was used for the synthesis of example 77.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143242B2
Source datasetuspto-grants-2012_03
ORD IDord-e032b30bfad946b0b2dd8cf22f063ac6
Source noteuspto-grants-2012_03