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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1658344Generated: November 2, 2026

ethyl 8-chloro[1,3]dioxolo[4,5-g]quinoline-7-carboxylate → Ethyl 8-ethoxy-2H-[1,3]dioxolo[4,5-g]quinoline-7-carboxylate

https://huagongshe.com/reaction/1658344

Reaction equation

Participants

RoleNameHCIDCharge
Reactantethyl 8-chloro[1,3]dioxolo[4,5-g]quinoline-7-carboxylateHCID 824579—
ReactantSodium ethoxideHCID 2723922—
SolventEthanolHCID 702—
ProductEthyl 8-ethoxy-2H-[1,3]dioxolo[4,5-g]quinoline-7-carboxylateHCID 12367717—

Reaction Steps

To a mixture containing 126 g of ethyl 4-chloro-6,7-methylenedioxyquinoline-3-carboxylate and 200 ml of absolute ethanol was added dropwise an ethanolic sodium ethylate solution prepared from 34 g of sodium ethylate and 250 ml of ethanol with stirring. The resulting mixture was refluxed for 1.5 hours and the ethanol was removed under reduced pressure. The residue was poured into ice-water, the insoluble solid was filtered, washed with water and dried to provide 126 g of almost pure ethyl 4-ethoxy-6,7-methylenedioxyquinoline-3-caboxylate, m.p. 84°-86°C. Recrystallization from petroleum ether gave colorless needles, m.p. 85°-85.5°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03963736
Source datasetuspto-grants-1976_06
ORD IDord-e3a8369334a64b4799716e09c59b6819
Source noteuspto-grants-1976_06