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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462462Generated: November 1, 2026

Pyridine → Ethyl 4-(methoxycarbonylmethoxy)acetoacetate

https://huagongshe.com/reaction/462462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
ReactantMethyl (2-chloro-2-oxoethoxy)acetateHCID 12361282—
SolventDichloromethaneHCID 6344—
ProductEthyl 4-(methoxycarbonylmethoxy)acetoacetateHCID 1345721712.3%

Reaction Conditions

Temperature5 °C

Reaction Steps

Methyl 2-(chloroformylmethoxy)acetate (216.6 g) was added over 45 minutes to a stirred solution of 2,2-dimethyl-1,3-dioxane-4,6-dione (173.9 g) and pyridine (189.6 g) in dichloromethane (1000 ml) keeping the temperature below 5° C. The mixture was stirred at 5° C. for 30 minutes, allowed to warm up to room temperature over one hour, washed with 2.4M hydrochloric acid and water, dried over magnesium sulphate and evaporated. The resulting brown oil was dissolved in ethanol (300 ml) and the solution heated under reflux for 2.5 hours and evaporated. The residual oil was distilled to give the title compound (32.5 g), b.p. 138°-140°/1 torr which was characterised by its N.m.r. spectrum in CDCl3, δ values: 4.27 (2H,s); 4.20 (2H, q, J 7 Hz); 4.16 (2H,s); 3.75 (3H, s); 3.54 (2H, s); 1.29 (3H, t, J 7 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04515799
Source datasetuspto-grants-1985_05
ORD IDord-96d5dc5cd7ea4545b5178e560b4f64b5
Source noteuspto-grants-1985_05