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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767418Generated: October 31, 2026

Ethyl bromoacetate → [(Quinolin-4-yl)oxy]acetic acid

https://huagongshe.com/reaction/1767418

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
Reactantquinolin-4-olHCID 178516385—
SolventAcetoneHCID 180—
Product[(Quinolin-4-yl)oxy]acetic acidHCID 2263368629.5%

Reaction Steps

The mixture of 4-hydroxyquinoline (290 mg, 2.0 mmol), potassium carbonate (910 mg, 6.6 mmol), ethyl bromoacetate (500 mg, 3.0 mmol) and acetone (25 ml) was refluxed for 8 h. After cooling, the mixture was filtered to remove potassium carbonate. The filtrate was concentrated under reduced pressure. To this residue, 10 ml dioxane and 14 ml 5% sodium hydroxide solution were added. After the mixture was stirred at room temperature overnight, it was acidified with concentrated hydrochloric acid to pH 3, and then extracted three times with ethyl acetate (20 ml each). Water layer was placed in cold room, and solid came out. The crystals were filtered with suction and washed with water, and then dried to give 120 mg quinoline-4-oxyacetic acid as gray crystals, mp 274-276° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE039707E1
Source datasetuspto-grants-2007_06
ORD IDord-1580b63e98db44aea6e2f127bcb02373
Source noteuspto-grants-2007_06