HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → Phenol, 4-(4-(methylsulfonyl)phenoxy)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Benzene, 1-methoxy-4-(4-(methylsulfonyl)phenoxy)- | HCID 514881 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Phenol, 4-(4-(methylsulfonyl)phenoxy)- | HCID 514882 | 98.9% |
Reaction Steps
A solution of 37.3 g of 4-(4-(methylsulfonyl)phenoxy)-1-methoxybenzene (Example 18), 41 ml of 48% aqueous hydrogen bromide and 185 ml of glacial acetic acid was heated at reflux under nitrogen for 21 hrs. The reaction mixture was cooled and the solvent removed in vacuo. The product was collected by filtration, washed well with water and dried, which gave 35.0 g (98.9% yield) of the product. Recrystallization from aqueous ethanol gave purified 4-(4-(methylsulfonyl)phenoxy)phenol, mp 129°-130° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04349568 |
| Source dataset | uspto-grants-1982_09 |
| ORD ID | ord-1acd3a1bdd854cf59d611823204970f6 |
| Source note | uspto-grants-1982_09 |