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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611928Generated: November 1, 2026

Diethyl (ethoxymethylene)malonate → HCID 22252500, compound

https://huagongshe.com/reaction/1611928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl (ethoxymethylene)malonateHCID 6871—
Reactant5-Amino-3-methylisoxazoleHCID 84590—
ProductHCID 22252500HCID 22252500—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 5-amino-3-methylisoxazole (5.26 g) and diethyl ethoxymethylenemalonate (10.9 ml) was heated at 120° C. for 3 hrs. The mixture was cooled to room temperature. The precipitated solid was collected, washed with n-hexane and dried under high vacuum. A portion of this solid (11.37 g) was dissolved in phosphoryl chloride (55 ml), heated at reflux for 11 hrs, and then cooled to room temperature. The mixture was concentrated under reduced pressure and the residue was purified with the column chromatography(ethyl acetate: n-hexane=1:9) to give ethyl 3-methylisoxazolo[5,4-b]pyridine-5-carboxylate as a white solid. Zinc powder (2.75 g) was added to a solution of a portion of the solid (2.43 g) in acetic acid (24 ml), the was stirred at 80° C. for 1.5 hrs, and then filtered. The filtrate was concentrated under reduced pressure. The residue was dissolved in a mixture of 5N NaOH (10 ml) and ethanol (10 ml), the solution was refluxed for 1.5 hrs, cooled to room temperature, and acidified with concentrated HCl. The precipitated solid was collected by the filtration, washed with water, and dried under high vacuum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06992086B2
Source datasetuspto-grants-2006_01
ORD IDord-7763fd0a8b4f409bb8c1b4af31778f03
Source noteuspto-grants-2006_01