HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → Phenol, 4-(5-octyl-2-pyridinyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 2-(4-Methoxyphenyl)-5-octylpyridine | HCID 14069921 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Phenol, 4-(5-octyl-2-pyridinyl)- | HCID 1725484 | — |
Reaction Steps
The 2-(p-methoxyphenyl)-5-octylpyridine was dissolved in 100 ml of acetic acid. 8 ml of 48% hydrobromic acid was added to the reaction solution and the solution was heated for 15 hours under reflux. 100 ml of water was added to the reaction solution and the organic layer was extracted with chloroform. After washing the extract three times with water, the chloroform was removed by distillation. The residue was recrystallized from a mixture of acetone and hexane to yield 8.3 g (0.029 mol) of 2-(p-hydroxyphenyl)-5-octylpyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04723018 |
| Source dataset | uspto-grants-1988_02 |
| ORD ID | ord-af619c8be0ee4e34923575da7dc53150 |
| Source note | uspto-grants-1988_02 |