HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635944Generated: October 30, 2026
Methyl acetoacetate → HCID 18673606, compound
https://huagongshe.com/reaction/1635944
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl acetoacetate | HCID 7757 | — |
| Reactant | 37630-26-5 | HCID 5381679 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Solvent | Ammonia | HCID 222 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 18673606 | HCID 18673606 | 59.8% |
Reaction Steps
0.69 g(5.9 mmol) of methyl 3-oxobutanoate and 1.08 g(5.9 mmol) of 1-[(E)-2-nitroethenyl]naphthalene were added to 2.37 ml of 0.5M sodium methoxide in methanol, and the resulting mixture was stirred for 2 hours at 0° C. The reaction solution was diluted with 10 ml of cold methanol, through which ammonia gas was passed. Reaction was carried out for 12 hours at 0° C. under stirring. After reaction was completed, the solvent was removed under reduced pressure and the residue was subjected to column chromatography(eluent: ethylacetate/hexane=90/10, v/v; ethylacetate/hexane=70/30, v/v) to give 936 mg(3.53 mmol, Yield 59%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06511978B1 |
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| Source dataset | uspto-grants-2003_01 |
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| ORD ID | ord-8b76108161264c74b3b2199b8efe58cd |
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| Source note | uspto-grants-2003_01 |
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