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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852982Generated: October 30, 2026

HCID 178469501, compound → HCID 178524706, compound

https://huagongshe.com/reaction/852982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178469501HCID 178469501—
SolventWaterHCID 962—
SolventPotassium HydroxideHCID 14797—
ProductHCID 178524706HCID 178524706100.5%

Reaction Steps

A suspension of 6-bromo-4-hydroxy-quinoline-3-carboxylic acid ethyl ester (102.59 g, 337.7 mmol) in 10% potassium hydroxide in water (689 mL) was heated to reflux for 5 h to afford a light brown solution. After cooling to room temperature, the undissolved solid particles were removed by filtration and the filtrate was extracted with dichloromethane to remove any neutral impurities. The aqueous layer was neutralized with 3.0N hydrochloric acid to afford a white precipitate. Then, the solids were collected by filtration and washed with water. After drying in air, 91 g (98% yield) of 6-bromo-4-hydroxy-quinoline-3-carboxylic acid was isolated as a white solid: EI-HRMS m/e calcd for C10H6BrNO3 (M+) 266.9531, found 266.9521.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253285B2
Source datasetuspto-grants-2007_08
ORD IDord-57c0c285785e4714a7a6c036720340b8
Source noteuspto-grants-2007_08