HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Anisidine → HCID 23359023, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | Ethyl 3-ethoxy-2-(2,3,4,5-tetrafluorobenzoyl)acrylate | HCID 54346083 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 23359023 | HCID 23359023 | 80.5% |
Reaction Steps
A mixture of ethyl 2-(2,3,4,5-tetrafluorobenzoyl)-3-ethoxyacrylate (0.4 g), p-anisidine (0.15 g) and ethanol (4 ml) is stirred at room temperature for 30 minutes. After the reaction, the solvent is distilled off under reduced pressure. To the residue is added anhydrous dioxane (10 ml) and thereto is further added portionwise 60% sodium hydride (60 mg). The mixture is stirred at room temperature for 30 minutes. The reaction mixture is poured into saturated aqueous ammonium chloride, and the mixture is extracted with dichloromethane to give ethyl 6,7,8-trifluoro-1-(4-methoxyphenyl)-1,4-dihydro-4-oxoquinoline-3-carboxylate (0.37 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04755513 |
| Source dataset | uspto-grants-1988_07 |
| ORD ID | ord-3f47cba2e3654375bef6823e0c5e7c91 |
| Source note | uspto-grants-1988_07 |