Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 23359023 | HCID 23359023 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 13912594 | HCID 13912594 | 87.6% |
Reaction Steps
A mixture of ethyl 6,7,8-trifluoro-1-(4-methoxyphenyl)-1,4-dihydro-4-oxoquinoline-3-carboxylate (0.37 g), conc. hydrochloric acid (1 ml) and 90% acetic acid (4 ml) is heated at 120° C. for one hour. After cooling, the precipitated crystals are separated by filtration, washed well with water and with a mixture of ethanol and ether to give 6,7,8-trifluoro-1-(4-methoxyphenyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid (0.3 g) as white crystals, m.p. 252°-254° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04684648 |
|---|
| Source dataset | uspto-grants-1987_08 |
|---|
| ORD ID | ord-9a8c22c9c71341ed95c00f59bcfa37b2 |
|---|
| Source note | uspto-grants-1987_08 |
|---|