HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → ethyl quinoline-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Quinaldic Acid | HCID 7124 | — |
| Product | ethyl quinoline-2-carboxylate | HCID 421739 | — |
Reaction Steps
29.89 g of quinoline-2-carboxylic acid were heated under reflux for 51/2 hours in 450 ml of ethanol with the addition of 3.5 ml of sulfuric acid. The reaction mixture was worked up by evaporating it, taking up the residue in water and extracting the mixture with dichloromethane. The organic phase was washed with aqueous sodium bicarbonate solution and then with water until neutral, dried and evaporated. 32.23 g of crude ethyl quinoline-2-carboxylate were obtained as a green oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05324725 |
| Source dataset | uspto-grants-1994_06 |
| ORD ID | ord-976e133b766b461e9cb7d0504ebe0de8 |
| Source note | uspto-grants-1994_06 |