HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 6-hydroxyquinoline-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 6-Hydroxyquinoline-2-carboxylic acid | HCID 13336780 | — |
| Product | Ethyl 6-hydroxyquinoline-2-carboxylate | HCID 57681568 | — |
Reaction Steps
6-Hydroxy-quinoline-2-carboxylic acid (2.3 g, 0.012 mol) was dissolved in absolute ethanol (150 ml). Sulfuric acid (0.550 ml, 0.0096 mol) was added and the mixture was refluxed for 16 hours. After cooling to room temperature the ethanol was evaporated and 60 ml of ethyl acetate, 50 ml of cooled water were added. The pH was adjusted to 7 with solid NaHCO3. Extraction and concentration of the organic phase gave the title product as a light yellow solid that was used for the next steps without purification (2.1 g, 81% of theory). MS (m/e)=218.4 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07534891B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-a9ed3583660647f3aa9bd5df695dae7e |
| Source note | uspto-grants-2009_05 |