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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633808Generated: October 27, 2026

Hydrochloric Acid → 3-Hydroxy-6-methoxyquinoline-4-carboxylic acid

https://huagongshe.com/reaction/633808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
Reactant5-MethoxyisatinHCID 38333—
ReactantChloropyruvic acidHCID 151137—
ReactantSodium BisulfiteHCID 23665763—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product3-Hydroxy-6-methoxyquinoline-4-carboxylic acidHCID 6571018221.5%

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 successively with a saturated sulfur dioxide aqueous solution and water, then purified by column chromatography (silica gel, eluent: ethyl acetate:acetonitrile:methanol, 70:5:5, v/v/v) to afford 3-hydroxy-6-methoxyquinoline-4-carboxylic acid as a light brown solid (2.66 g, 21% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321788B2
Source datasetuspto-grants-2016_04
ORD IDord-3de60a8a52684cc7b136d0f2346f7ddd
Source noteuspto-grants-2016_04