HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium ethoxide → Ethyl 1-Ethyl-2,4-dioxopiperidine-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | ethyl N-ethoxycarbonylacetyl-3-ethylaminopropionate | HCID 13784117 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 1-Ethyl-2,4-dioxopiperidine-3-carboxylate | HCID 13784118 | 71% |
Reaction Steps
5.8 g of metallic sodium was added to 300 ml of ethanol and they were reacted to obtain an ethanol solution containing sodium ethoxide. To this solution was added 62.2 g of ethyl N-ethoxycarbonylacetyl-3-ethylaminopropionate, and they were refluxed for 4 hours and allowed to cool. Ethanol was distilled off. Thereto were added ethyl acetate and a dilute aqueous hydrochloric acid solution and the resulting mixture was shaken. The organic layer was separated, water-washed, dried and concentrated to obtain 36.3 g of 3-carboethoxy-1-ethylpiperidine-2,4-dione as an oily matter with an yield of 71%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04742165 |
| Source dataset | uspto-grants-1988_05 |
| ORD ID | ord-1fd6fe2772494ec993726d59493f8be5 |
| Source note | uspto-grants-1988_05 |