HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107146Generated: October 31, 2026
Ethyl Acetoacetate → HCID 23047731, compound
https://huagongshe.com/reaction/2107146
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | HCID 10753909 | HCID 10753909 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 23047731 | HCID 23047731 | — |
Reaction Steps
A solution of 6.0 g (46 mmol) of ethyl acetoacetate in 6 ml of absolute ethanol is added drop by drop, with stirring, to a solution of 23 mmol of sodium ethylate in 18 ml of ethanol. Stirring is continued for another 15 minutes to complete the salt formation, and then a solution of 6.0 g (23 mmol) of 5-(4-chlorophenyl)pentyl bromide in 6 ml of absolute ethanol is added. The mixture is then heated for 3 hours with refluxing, and then completely concentrated by evaporation. Water is added to the concentrate and the mixture is neutralized with 2N hydrochloric acid. Then the organic components are extracted with ether, the combined extracts are dried, and are concentrated by evaporation. The concentrate is chromatographed on silica gel with a mixture of n-heptane and butanone. Yield: 5.8 g (81% of theory) of ethyl 2-acetyl-7-(4-chlorophenyl)heptanoate, a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04933367 |
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| Source dataset | uspto-grants-1990_06 |
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| ORD ID | ord-8c33e973386c4c259a9a9d8849ed8177 |
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| Source note | uspto-grants-1990_06 |
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