HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-Benzyloxy-4-chloro-6-methoxyquinoline hydrochloride → 4-Chloro-6-methoxyquinolin-7-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-Benzyloxy-4-chloro-6-methoxyquinoline hydrochloride | HCID 22646561 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 4-Chloro-6-methoxyquinolin-7-ol | HCID 135583731 | 98% |
Reaction Steps
A solution of 7-benzyloxy-4-chloro-6-methoxyquinoline hydrochloride (6.8 g, 20 mmol) in TFA (80 ml) was heated at reflux for 5.5 hours. The volatiles were removed by evaporation, the residue suspended in water and the mixture was adjusted to pH7 with a saturated aqueous sodium hydrogen carbonate solution. The resulting solid was collected by filtration, washed with water, ether and dried under vacuum to give 4-chloro-7-hydroxy-6-methoxyquinoline (4.1 g, 98%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06809097B1 |
| Source dataset | uspto-grants-2004_10 |
| ORD ID | ord-a07b263e1f9c44569f87333c7a7d219b |
| Source note | uspto-grants-2004_10 |