HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron trifluoride → Methyl 6-hydroxyquinoline-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron trifluoride | HCID 6356 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 6-Hydroxyquinoline-5-carboxylic acid | HCID 16042481 | — |
| Product | Methyl 6-hydroxyquinoline-5-carboxylate | HCID 19077292 | — |
Reaction Steps
6-Hydroxy-5-quinolinecarboxylic acid [as reported by Da Re, P. et al. in Ann. Chem. (Rome) 1970, 60(3), 215-24 (C.A. 73, 25338m)] is reacted with methanolic boron trifluoride solution for several hours. The resulting mixture is added to an aqueous solution of sodium bicarbonate to give finally a basic solution. The solution is extracted with chloroform. The chloroform extract is dried over anhydrous sodium sulfate and concentrated and the residue is crystallized from a suitable solvent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04705853 |
| Source dataset | uspto-grants-1987_11 |
| ORD ID | ord-855081256c614ffda0966da5615eb24a |
| Source note | uspto-grants-1987_11 |