HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Hydroxyquinoline → Dimethyl Ether
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Hydroxyquinoline | HCID 6038 | — |
| Reactant | Swietenidin B | HCID 442933 | — |
| Reactant | 8-methoxy-3-methoxy-4-hydroxy-1-methyl-2(1H)-quinolinone | HCID 54723908 | — |
| Product | Dimethyl Ether | HCID 8254 | — |
| Product | 3,4,8-Trimethoxy-1-methylquinolin-2(1H)-one | HCID 21715161 | — |
Reaction Steps
As compounds having substituent groups on the aromatic ring of a quinolinone, Indian J. Chem., Sect. B, 15B(5), pp. 440-444, 1977, discloses 3,4-dimethoxy-2(1H)-quinolinone, 8-methoxy-3-methoxy-4-hydroxy-1-methyl-2(1H)-quinolinone, and a methyl ether thereof, 8-methoxy-3,4-dimethoxy-1-methyl-2(1H)-quinolinone as compounds obtained from the bark of Chloroxylon swietenia DC.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06136822 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-c169d93c5ea845459ea77f652eaa0676 |
| Source note | uspto-grants-2000_10 |