HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224477Generated: October 30, 2026
Dimethyl Sulfoxide → 4-(4-Fluorophenylsulphonyl)phenol
https://huagongshe.com/reaction/224477
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Benzene, 1,1'-sulfonylbis(4-fluoro- | HCID 67842 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(4-Fluorophenylsulphonyl)phenol | HCID 343802 | — |
Reaction Steps
Bis-(4-fluorophenyl) sulphone (100 g; 0.394 mole), potassium hydroxide solution (91.98 g; 0.787 mole KOH) and dimethyl sulphoxide (400 cm3) were stirred together in a stainless steel vessel under nitrogen at 57° C. for 24 hours. Two liquid phases remained throughout the reaction. The reaction mixture was diluted with water and twice extracted with diethyl ether to recover non-phenolic material (9 g). The aqueous phase was then acidified and the phenolic component (86 g; m.p. 150°-154° C.) was extracted with more ether. By subliming this product under a diffusion pump at 180° C., followed by recrystallisation from toluene (400 cm3), 4-(4-fluorophenylsulphonyl)phenol (72.5 g) was obtained, m.p. 158°-159° C. The potassium salt was obtained from this phenol as a very pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04232142 |
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| Source dataset | uspto-grants-1980_11 |
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| ORD ID | ord-6f1659897777421c8377ceedab2a16c3 |
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| Source note | uspto-grants-1980_11 |
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