HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-Fluoro-4-(phenyl sulfonyl)benzeneamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | Potassium Permanganate | HCID 516875 | — |
| Reactant | 3-Fluoro-4-(phenylthio)nitrobenzene | HCID 14926325 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-Fluoro-4-(phenyl sulfonyl)benzeneamine | HCID 10753234 | 75% |
Reaction Steps
To a stirred solution of 3-fluoro-4-(phenylthio)nitrobenzene (5.65 g, 22.7 mmol) in glacial acetic acid (200 mL) was added potassium permanganate (4.30 g, 27.2 mmol) in distilled water (75 mL). The dark brown mixture was stirred at room temperature for 1 hour, then treated with solid sodium sulfite until the solution clarified. The mixture was diluted with water and filtered to yield an off-white solid. Recrystallization from absolute ethanol yielded the title sulfone (4.80 g, 75%) as an off-white solid; mp 124°-125° C. 1H-NMR (300 MHz, DMSO-d6): 7.68-7.73 (m, 2H, aromatic) 7.79-7.84 (m, 1H, aromatic) 8.00 (d, 2H, J=8.2 Hz, aromatic) 8.28-8.38 (m, 3H, aromatic). MS (CI, CH4): 282 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05567735 |
| Source dataset | uspto-grants-1996_10 |
| ORD ID | ord-6c8b3f09ae10464484a464426d6283a4 |
| Source note | uspto-grants-1996_10 |