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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1244806Generated: October 27, 2026

Water → Ethyl 2-(6-quinolinyloxy)-2-(ethoxy)acetate

https://huagongshe.com/reaction/1244806

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant6-HydroxyquinolineHCID 11374—
ReactantEthyl 2-chloro-2-ethoxyacetateHCID 2724873—
ReactantPotassium tert-butoxideHCID 23665647—
CatalystPotassium IodideHCID 4875—
Solventtert-ButanolHCID 6386—
ProductEthyl 2-(6-quinolinyloxy)-2-(ethoxy)acetateHCID 2192312364.7%

Reaction Steps

Potassium t-butoxide (3.15 g) was dissolved in t-butyl alcohol (20 ml) and stirred for 10 minutes at ambient temperature. 6-Hydroxyquinoline (3.0 g) was added, the resulting dark green solution was stirred for 15 minutes, and then ethyl 2-chloro-2-ethoxyacetate (4.22 g, 90% pure) added, followed by a catalytic amount of potassium iodide (0.005 g). The mixture was stirred for 18 hours, poured into water and extracted with chloroform. The organic fraction was washed with brine, water, and dried over magnesium sulphate. The solvent was evaporated to give a brown oil, which was purified by flash chromatography on silica gel, eluting with a gradient of ethyl acetate:hexane (1:2 to 4:1) to give ethyl 2-(6-quinolinyloxy)-2-(ethoxy)acetate as a pale brown oil (3.68 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07122672B2
Source datasetuspto-grants-2006_10
ORD IDord-a0565f49269a425281f6f6cc06816d80
Source noteuspto-grants-2006_10