HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 7-Methylquinolin-6-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 6-Methoxy-7-methylquinoline | HCID 15534898 | — |
| Solvent | Bromic acid | HCID 24445 | — |
| Product | 7-Methylquinolin-6-ol | HCID 12838956 | 47.2% |
Reaction Steps
6-Methoxy-7-methyl-quinoline (3 g) was added to an aqueous bromic acid solution (30 ml), and the mixture was heated under reflux for 7 hr. The reaction solution was cooled to room temperature, the aqueous layer was then neutralized with an aqueous sodium hydroxide solution and an aqueous sodium hydrogencarbonate solution. The organic layer was extracted with ether, the solvent was removed by distillation under the reduced pressure, and the residue was washed with cooled ether to give 6-hydroxy-7-methylquinoline (1.3 g, yield 47%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07560558B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-a88db85475c740678b93231be4afa665 |
| Source note | uspto-grants-2009_07 |