HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2-(6,7-Dimethoxyquinolin-4-yloxy)-5-methoxybenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Ethyl 2-(6,7-dimethoxyquinolin-4-yloxy)-5-methoxybenzoate | HCID 23078318 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(6,7-Dimethoxyquinolin-4-yloxy)-5-methoxybenzoic acid | HCID 23078521 | 105.6% |
Reaction Steps
Ethyl 2-(6,7-dimethoxyquinolin-4-yloxy)-5-methoxybenzoate (143 mg) and lithium hydroxide (78 mg) were suspended in a mixed solvent composed of ethanol (10 ml) and water (1 ml), and the suspension was stirred at room temperature overnight. The solvent was then removed therefrom by distillation under the reduced pressure. Water was added to the residue, and the resultant solution was neutralized with 12N hydrochloric acid. The mixture was then extracted with chloroform. The chloroform layer was washed with water and saturated brine and was dried over anhydrous sodium sulfate. The solvent was removed therefrom by distillation under the reduced pressure to give the title compound (140 mg, yield 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07560558B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-3652b072d3e8418799d34a83a04ef576 |
| Source note | uspto-grants-2009_07 |