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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1589149Generated: November 2, 2026

2,2-Dimethyl-1,3-dioxane-4,6-dione → Ethyl 4-{[4-(2-chlorophenyl)-3-ethoxycarbonyl-5-methoxycarbonyl-6-methyl-1,4-dihydropyridin-2-yl]methoxy}acetoacetate

https://huagongshe.com/reaction/1589149

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
ReactantSodium hydrideHCID 24758—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantSodiumHCID 5360545—
Reactant{[4-(2-Chlorophenyl)-3-(ethoxycarbonyl)-5-(methoxycarbonyl)-6-methyl-1,4-dihydropyridin-2-yl]methoxy}acetic acidHCID 13457220—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-{[4-(2-chlorophenyl)-3-ethoxycarbonyl-5-methoxycarbonyl-6-methyl-1,4-dihydropyridin-2-yl]methoxy}acetoacetateHCID 70044209—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 2-{[4-(2-chlorophenyl)-3-ethoxycarbonyl-5-methoxycarbonyl-6-methyl-1,4-dihydropyridin-2-yl]methoxy}acetic acid (4.24 g) in tetrahydrofuran (60 ml) was treated with ice-cooling with carbonyldiimidazole (1.70 g) and the mixture stirred at 0° C. for 2.25 hours. This solution was added dropwise over 10 minutes to a solution of the sodium salt of 2,2-dimethyl-1,3-dioxane-4,6-dione in dimethylformamide (prepared by stirring a mixture of 2,2-dimethyl-1,3-dioxane-4,6-dione (1.44 g) and sodium hydride (0.30 g; 80% dispersion in oil) in dimethylformamide (30 ml) with ice-cooling for 30 minutes) and the mixture stirred for 16 hours at room temperature and then evaporated. The residue was dissolved in dichloromethane, washed twice with 1M hydrochloric acid and water, dried (MgSO4), and evaporated. A solution of the residual oil (6 g) in ethanol (50 ml) was heated under reflux for 6 hours and evaporated. The residue was dissolved in diethyl ether, washed twice with 10% aqueous sodium carbonate and once with saturated aqueous sodium chloride, dried (MgSO4), and evaporated. The residue was purified by chromatography on silica (30 g) using hexane plus 5-15% v/v ethyl acetate as eluant. Appropriate fractions were combined and evaporated and the residue crystallised from ethanol to give the title compound (1.5 g), m.p. 88°-89° C. Found: C,58.18; H,5.73; N,2.85. C24H28ClNO8 requires: C,58.36; H,5.71; N,2.84%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04568677
Source datasetuspto-grants-1986_02
ORD IDord-05d0459c391c48d890731c91d3bec0f0
Source noteuspto-grants-1986_02