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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851085Generated: October 31, 2026

Diethyl (ethoxymethylene)malonate → HCID 13188588, compound

https://huagongshe.com/reaction/851085

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl (ethoxymethylene)malonateHCID 6871—
ReactantHCID 13188587HCID 13188587—
ReactantBenzoxazinesHCID 17845026—
SolventWaterHCID 962—
ProductHCID 13188588HCID 1318858867%

Reaction Steps

A mixture of 1.11 g (5.5 mmols) of 7-chloro-8-fluoro-3-methyl-2,3-dihydro-4H-1,4-benzoxazine and 1.4 g (6.2 mmols) of diethyl ethoxymethylenemalonate was stirred for 2 hours while heating at 130°-140° C. (bath temperature). After confirming disappearance of the starting benzoxazine compound by thin-layer chromatography, 5 g of ethyl polyphosphate was added to the reaction mixture and the mixture was again allowed to react for 1 hour at 140° C. (bath temperature). After cooling, 20 ml of water was added to the mixture and the precipitate formed was extracted with 150 ml of chloroform. The chloroform extract was dried with sodium sulfate and chloroform was then distilled off. The resulting residue was purified by silica gel (20 g) column chromatography using methanol-chloroform (5:95 by volume) as an eluant to provide 1.2 g (67.0% yield) of ethyl 9-chloro-10-fluoro-3-methyl-7-oxo-2,3-dihydro-7H-pyrido[1,2,3-de][1,4]benzoxazine-6-carboxylate with m.p. 263°-264° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04382892
Source datasetuspto-grants-1983_05
ORD IDord-a77555a6d3d346c5811767907dd791fb
Source noteuspto-grants-1983_05