HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl benzoylacetate → HCID 20156557, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl benzoylacetate | HCID 7170 | — |
| Reactant | 2-Vinylpyridine | HCID 7521 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 20156557 | HCID 20156557 | 90.5% |
Reaction Steps
A sample of 120 g (0.62 mole) of ethyl benzoylacetate was added to 1.44 g (0.062 mole) of sodium and 32.8 g (0.31 mole) of 2-vinylpyridine added under an atmosphere of nitrogen. The mixture was heated with mechanical stirring on the steam bath for 17 h. After cooling the reaction mixture to room temperature, 100 mL of 3N hydrochloric acid was added, and the aqueous mixture washed with ether. The hydrochloric acid layer was made basic with 10% potassium carbonate solution, and extracted with ether. The ether layer was washed with brine, dried (MgSO4), and the ether evaporated in vacuo to give 83.4 g (90% yield) of the crude title compound as a red oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04716172 |
| Source dataset | uspto-grants-1987_12 |
| ORD ID | ord-f89c717ba3b648d39b8aa65770dadf93 |
| Source note | uspto-grants-1987_12 |