Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | HCID 23359023 | HCID 23359023 | — |
| Product | HCID 13912595 | HCID 13912595 | 79.1% |
Reaction Steps
A mixture of ethyl 6,7,8-trifluro-1-(4-methoxyphenyl)-1,4-dihydro-4-oxoquinoline-3-carboxylate (0.37 g) and 47% hydrobromic acid (4 ml) is heated at 120° C. for 3 hours. After cooling, the precipitated crystals are separated by filtration, washed with water and further with a mixture of ethanol and ether to give 6,7,8-trifluoro-1-(4-hydroxyphenyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid (0.26 g), m.p. >300° C., white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04684648 |
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| Source dataset | uspto-grants-1987_08 |
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| ORD ID | ord-705267c2952f4b7e8eb49b392fb3da0d |
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| Source note | uspto-grants-1987_08 |
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