HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422886Generated: October 26, 2026
Hydrochloric Acid → 3-Hydroxy-6-methoxyquinoline-4-carboxylic acid
https://huagongshe.com/reaction/1422886
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 5-Methoxyisatin | HCID 38333 | — |
| Reactant | Chloropyruvic acid | HCID 151137 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Hydroxy-6-methoxyquinoline-4-carboxylic acid | HCID 65710182 | 21.5% |
Reaction Steps
3-Chloro-2-oxo-propionic acid (11.46 g, 91.10 mmol, 1.61 eq) is added portionwise at room temperature to a stirred solution of 5-methoxy-1H-indole-2,3-dione (10.0 g, 56.45 mmol, 1.0 eq) and potassium hydroxide (30.5 g, 543.6 mmol, 9.6 eq) in water (60 mL). After 6 days stirring at room temperature, a solution of sodium hydrogen sulfite (2.3 g, 22.10 mmol, 0.4 eq) in water (4 mL) is added and the reaction mixture is acidified by the addition of concentrated hydrochloric acid (12N, 30 mL). The resulting yellow precipitate is collected by filtration, washed with a saturated sulfur dioxide aqueous solution and water, then purified by column chromatography (silica gel, eluent:ethyl acetate:acetonitrile:methanol:water, 70:5:2.5:2.5, v/v/v/v) to afford 3-hydroxy-6-methoxyquinoline-4-carboxylic acid as a light brown solid (2.66 g, 21% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08927541B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-e836f5b5e2924bc581c96d7ece0f519b |
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| Source note | uspto-grants-2015_01 |
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