HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462462Generated: November 1, 2026
Pyridine → Ethyl 4-(methoxycarbonylmethoxy)acetoacetate
https://huagongshe.com/reaction/462462
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2,2-Dimethyl-1,3-dioxane-4,6-dione | HCID 16249 | — |
| Reactant | Methyl (2-chloro-2-oxoethoxy)acetate | HCID 12361282 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 4-(methoxycarbonylmethoxy)acetoacetate | HCID 13457217 | 12.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04515799 |
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| Source dataset | uspto-grants-1985_05 |
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| ORD ID | ord-96d5dc5cd7ea4545b5178e560b4f64b5 |
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| Source note | uspto-grants-1985_05 |
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