HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1717282Generated: November 4, 2026
Ethyl Acetoacetate → HCID 68517178, compound
https://huagongshe.com/reaction/1717282
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | HCID 86629802 | HCID 86629802 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 68517178 | HCID 68517178 | 28% |
Reaction Steps
To a solution of 4-azido-5-chloro-N-ethyl-2-methoxybenzamide (1.0 g) obtained in Example 73b) and ethyl 3-keto-n-butanoate (0.61 ml) in ethanol (20 ml) was added 20% sodium ethoxide in ethanol solution (1.85 ml) at room temperature, and the mixture was stirred at 60° C. for 5 hr. The reaction mixture was cooled to room temperature, and the solvent was evaporated under reduced pressure. The residue was diluted with water and washed with ethyl acetate. The aqueous layer was acidified with 1N hydrochloric acid and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure to give the title compound as a pale-brown solid (0.38 g, 28%). The obtained crude product was used for the next reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07803822B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-00d04b8c801a478396bb82a9f22ec9e9 |
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| Source note | uspto-grants-2010_09 |
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