HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098756Generated: October 30, 2026
3'-(Trifluoromethylthio)acetophenone → HCID 59506285, compound
https://huagongshe.com/reaction/1098756
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3'-(Trifluoromethylthio)acetophenone | HCID 2777838 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59506285 | HCID 59506285 | 44% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08143242B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-e032b30bfad946b0b2dd8cf22f063ac6 |
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| Source note | uspto-grants-2012_03 |
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