HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1686403Generated: November 1, 2026
Water → 1,2-Difluoro-4-phenylsulfonylbenzene
https://huagongshe.com/reaction/1686403
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Reactant | 3,4-Difluorophenyl phenyl sulfide | HCID 66734083 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1,2-Difluoro-4-phenylsulfonylbenzene | HCID 26986177 | — |
Reaction Steps
3,4-difluoroaniline (3.5 g), acetonitrile (60 ml), diphenyldisulfide (6 g) and isoamyl nitrite (8 ml) were charged to a flask and heated at 60° C. for 2 h then evaporated under reduced pressure. The residue was purified by flash column chromatography (eluent isohexane) to give the subtitle compound. The product (3,4-difluorophenyl phenyl sulfide) was dissolved in acetonitrile (60 ml). Water (10 ml) and oxone (20 g) were added and stirred for 72 h at RT. The reaction mixture was partitioned between ether/water, the organics were separated, washed with water, then dried (MgSO4) and evaporated under reduced pressure. The residue was purified by flash column chromatography (eluent 5-10% ethyl acetate/isohexane) to give the subtitle compound (2.14 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08148572B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-302f30126da6495984bc2f12ed333f21 |
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| Source note | uspto-grants-2012_04 |
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