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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090135Generated: November 2, 2026

Diethyl (ethoxymethylene)malonate → HCID 21829132, compound

https://huagongshe.com/reaction/1090135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl (ethoxymethylene)malonateHCID 6871—
Reactantp-Phenetidine, 3-methoxy-HCID 209360—
ProductHCID 21829132HCID 2182913255.2%

Reaction Steps

4-Ethoxy-3-methoxyaniline (2.6 g) and diethyl ethoxymethylenemalonate (3.4 g) were reacted in the same manner as in Experimental Example 1 to obtain 6-ethoxy-3-ethoxycarbonyl-7-methoxy-4(1H)-quinolone (2.5 g). The compound (2.3 g) was ethylated with potassium carbonate (3.3 g) and ethyl iodide (6.1 g) in the same manner as in Experimental Example 9 to obtain 6-ethoxy-3-ethoxycarbonyl-1-ethyl-7-methoxy-4(1H)-quinolone (1.8 g). This compound (1.4 g) was hydrolyzed in the same manner as in Experimental Example 9 to obtain a carboxylic acid (1.2 g), which was then decarboxylated in the same manner as in Experimental Example 9 to obtain 6-ethoxy-1-ethyl-7-methoxy-4(1H)-quinolone (compound 49, 210 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05081121
Source datasetuspto-grants-1992_01
ORD IDord-4c797cd740794b8eaae4557ec0696953
Source noteuspto-grants-1992_01