HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243424Generated: October 31, 2026
Ethyl Acrylate → Ethyl 5-acetyl-4-oxohexanoate
https://huagongshe.com/reaction/1243424
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | Acetylacetone | HCID 31261 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 3,5-dimethyl-4-(4-methylpiperazine-1-carbonyl)-1H-pyrrole-2-carbaldehyde | HCID 12111582 | — |
| Catalyst | Sodium | HCID 5360545 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 5-acetyl-4-oxohexanoate | HCID 13545064 | — |
Reaction Steps
Sodium metal (1 5 g) was placed in a 3 L 3 neck round bottom flask equipped with a thermometer, reflux condenser and mechanical stirring and placed in an oil bath. Absolute ethanol (1 L) was added with stirring. When the sodium had dissolved, 350 g of pentan-2,4-dione was added all at once and then 310 g of ethyl acrylate added over 30 minutes. The mixture was refluxed for 2.5 hours and then allowed to cool to room temperature overnight. Glacial acetic acid (3 mL) was added and the solvent removed by rotary evaporation. The residue was filtered through a pad of diatomaceous earth and distilled in a wiped film still at 0.1 mm. The distillate was redistilled using a 10 inch vacuum jacketed Vigreux column to give 518 g of ethyl 5-acetyl-4-oxohexanoate, BP 84-92° C. at 0.2-0.7 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07119090B2 |
|---|
| Source dataset | uspto-grants-2006_10 |
|---|
| ORD ID | ord-adc82151c810466f8defdb4fab7242d3 |
|---|
| Source note | uspto-grants-2006_10 |
|---|