HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2-(Furan-2-yl)quinoline-4-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Isatin | HCID 7054 | — |
| Reactant | 2-Acetylfuran | HCID 14505 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(Furan-2-yl)quinoline-4-carboxylic acid | HCID 697640 | — |
Reaction Steps
5 g (34.0 mmol) of isatin, 4 ml (40.8 mmol) of 2-acetylfuran and 6.3 g (112.2 mmol) of potassium hydroxide were dissolved in 40.9 ml of abs. EtOH and the slurry heated at 80° C. for 12 hours. After cooling of the reaction mixture, 50 ml of water were added and the solution extracted with 50 ml of Et2O. The ice-cooled aqueous phase was acidified to pH 1 with 37% HCl and the precipitate collected by filtration and washed with water. The crude product obtained was dried in-vacuo at 40° C. to yield 8.5 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05811553 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-5de8f06a00b242d1865ae7d774c3de22 |
| Source note | uspto-grants-1998_09 |