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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573422Generated: October 30, 2026

Diethyl (ethoxymethylene)malonate → HCID 89582867, compound

https://huagongshe.com/reaction/573422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl (ethoxymethylene)malonateHCID 6871—
ReactantEthyl isocyanateHCID 8022—
Reactant4-FluoroanilineHCID 9731—
ReactantSodium ethoxideHCID 2723922—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 89582867HCID 8958286725%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-fluoroaniline (1.0 g, 9.01 mmol) in THF (20 mL) at 0° C., was slowly added ethyl isocyanate (0.70 g, 10.0 mmol). After stirring 30 min. at 0° C., the solution was warmed to rt and the solvent was removed under vacuum. To the residue was added ethanol (30 mL), diethyl ethoxymethylenemalonate (1.95 g, 9.01 mmol) and 21% NaOEt in ethanol (2.92 mL, 9.01 mmol)) and the reaction stirred 48 h at rt. The solvent was removed under vacuum and cold conc. HCl was added to pH 6. The aqueous layer was removed under vacuum and the solids were crystallized from ethyl acetate and hexanes. 3-Ethyl-1-(4-fluorophenyl)-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidine-5-carboxylic acid ethyl ester isomer was isolated in 25% yield. 1H NMR (CDCl3) δ: 8.32 (s, 1H), 7.20-7.14 (m, 4H), 4.35 (q, 2H, J=7.1 Hz), 3.95 (q, 2H, J=7.2 Hz), 1.42 (t, 3H, J=7.2 Hz), 1.36 (t, 3H, J=7.2 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029538B2
Source datasetuspto-grants-2015_05
ORD IDord-29da791db95f441cb2cd826f19b38210
Source noteuspto-grants-2015_05