HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486924Generated: October 31, 2026
Hydrochloric Acid → 6-Bromo-4-hydroxyquinoline-3-carboxylic acid
https://huagongshe.com/reaction/1486924
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 6-bromo-4-oxo-1,4-dihydroquinoline-3-carboxylate | HCID 689824 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-Bromo-4-hydroxyquinoline-3-carboxylic acid | HCID 693203 | 96% |
Reaction Steps
2N Sodium hydroxide (506 mL, 1011.43 mmol) was added to a stirred suspension of ethyl 6-bromo-4-oxo-1H-quinoline-3-carboxylate (59.9 g, 202.29 mmol) in EtOH (590 mL) and the resulting solution stirred at 75° C. for 1.5 h. Water was added and the mixture cooled to 0° C. The pH of the solution was adjusted to 3 using hydrochloric acid and the precipitate collected by filtration. The solid was washed with water, EtOH/water (1:1) then Et2O before being dried to afford the desired material (51.9 g, 96%) as a beige solid. NMR Spectrum: 1H NMR (500 MHz, DMSO-d6) δ 7.80 (1H, d), 8.05 (1H, d), 8.37 (1H, s), 8.93 (1H, s). Mass Spectrum: m/z (ES+)[M+H]+=270.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09428503B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-536a122401e9426489b5b677dc4e9482 |
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| Source note | uspto-grants-2016_08 |
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