HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl benzoylacetate → HCID 178487676, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl benzoylacetate | HCID 7170 | — |
| Reactant | 3-Methoxyaniline | HCID 10824 | — |
| Reactant | 4-Chloro-7-methoxy-2-phenylquinoline | HCID 10754477 | — |
| Product | HCID 178487676 | HCID 178487676 | — |
Reaction Steps
2-Phenyl-4-chloro-7-methoxy-quinoline can be prepared according to Scheme XXXXI. Ethyl benzoylacetate and m-anisidine can reacted together under thermal conditions to afford 2-phenyl-4-hydroxy-7-methoxy-quinoline in the presence of an acid, such as hydrochloric acid and the like. 2-Phenyl-4-hydroxy-7-methoxy-quinoline can be converted to 2-phenyl-4-chloro-7-methoxy-quinoline using a chlorinating agent. For example, the chlorinating can be P(O)Cl3, P(O)Cl3 with PCl5, and the like.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08048862B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-2a843adc474e4945b4a886fdca6b2f40 |
| Source note | uspto-grants-2011_11 |