HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 3'-Nitro-[1,1'-biphenyl]-4-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | 4'-Methoxy-3-nitro-1,1'-biphenyl | HCID 11138924 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3'-Nitro-[1,1'-biphenyl]-4-ol | HCID 12465087 | 94.1% |
Reaction Steps
Solid 4-methoxy-3'-nitrobiphenyl (1.63 g) was dissolved in acetic acid (25 ml) and then concentrated hydrobromic acid (48%, 25 ml) was added (CAUTION). The mixture was heated at reflux for 2 hours and was then cooled. The reaction mixture was partitioned between ether and water. The organic layer was dried over anhydrous magnesium sulfate, the solution filtered and concentrated under reduced pressure. The residue was purified by column chromatography over silica eluting with hexane:ether (9:1) to give the sub-title compound as a yellow oil (1.44 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05977105 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-65730d28c16e4690acb228ee744b53a2 |
| Source note | uspto-grants-1999_11 |