HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 3,8-Dimethoxy quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3-Quinolinol, 8-methoxy- | HCID 11084389 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3,8-Dimethoxy quinoline | HCID 10583798 | 87.3% |
Reaction Steps
175 mg of 3-hydroxy-8-methoxy quinoline [compound (V)] prepared in example 6 and 66 mg of potassium hydroxide were added to 3 ml of ethanol, and the solution was agitated for 30 minutes. To the solution was added 284 mg of iodomethane, and the solution was agitated for 24 hours. The solvent was removed, and the solution was extracted with dichloromethane. The dichloromethane layer was washed with water and aqueous sodium hydroxide, and dried with anhydrous magnesium sulfate. The dichloromethane was removed by vacuum distillation to give 165 mg of 3,8-dimethoxy quinoline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05824689 |
| Source dataset | uspto-grants-1998_10 |
| ORD ID | ord-aaf958ebc6be4ebdac4f38df1b6371fc |
| Source note | uspto-grants-1998_10 |