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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700252Generated: November 1, 2026

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

https://huagongshe.com/reaction/1700252

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 of dioxane and 14 ml 5% sodium hydroxide solution was 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 numberUS06350756B1
Source datasetuspto-grants-2002_02
ORD IDord-4469fc053b264f18bfd07731e0b98434
Source noteuspto-grants-2002_02