HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2119677Generated: November 2, 2026
Acetone → 3-(4-Fluorophenyl)-4-(2-fluoro-4-methylsulfonylphenyl)-2,5-dihydro-2-furanone
https://huagongshe.com/reaction/2119677
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetone | HCID 180 | — |
| Reactant | HCID 9858171 | HCID 9858171 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(4-Fluorophenyl)-4-(2-fluoro-4-methylsulfonylphenyl)-2,5-dihydro-2-furanone | HCID 9946385 | 85% |
Reaction Steps
To a solution of 3-(4-fluorophenyl)-4-(2-fluoro-4-methylsulfanylphenyl)-2,5-dihydro-2-furanone (6 g, 18.8 mmol) (obtained in step 2) in acetone (150 ml) was added a solution of oxone (34.8 g, 56.6 mmol) in water (75 ml). The reaction mixture was stirred vigorously for 2 h at 25° C. After completion of the reaction solvent was removed under low vacuum and water (200 ml) was added to it. The mixture was then extracted with EtOAc (2×100 ml), organic layers collected, combined, dried over anhydrous Na2SO4 and concentrated under vacuum. The crude product was then treated with MeOH (2×20 ml) and filtered to give 5.6 g of title compound in 85% yield as off white powder. m.p. 160°-162° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06686390B2 |
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| Source dataset | uspto-grants-2004_02 |
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| ORD ID | ord-8a4f6880254842a1ba4287313d2868d3 |
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| Source note | uspto-grants-2004_02 |
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