HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2085380Generated: October 30, 2026
Acetic Acid → Methyl 2-{(benzofuran-5-yl)methylene}-3-oxobutyrate
https://huagongshe.com/reaction/2085380
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Methyl acetoacetate | HCID 7757 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Benzo(c)(1,2,5)oxadiazole-5-carbaldehyde | HCID 2776296 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Methyl 2-{(benzofuran-5-yl)methylene}-3-oxobutyrate | HCID 54375059 | — |
Reaction Steps
A mixture of 5-formylbenzofurazan (0.60 g, 4.1 mmol), methyl acetoacetate (0.52 g, 4.5 mmol), piperidine (0.019 g, 0.23 mmol), and acetic acid (0.014 g, 0.23 mmol) in benzene (30 mL) was heated at reflux temperature (equipped with a Dean-Stark trap) for 8 h. Benzene was evaporated in vacuo, the residue was dissolved in ethyl acetate (80 mL) and washed with brine (50 mL), saturated potassium bisulfate solution (50 mL), and saturated sodium bicarbonate solution. The ethyl acetate solution was dried over magnesium sulfate, the solvent removed under reduced pressure and the residue was purified by column chromatography (EtOAc/hexane, 1/9 to 3/20). The desired product was obtained as oil (0.98 g, 98%) and was used in the next step without any further characterization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06720324B2 |
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| Source dataset | uspto-grants-2004_04 |
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| ORD ID | ord-0b356dcec6c2430890841d209ca78ab6 |
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| Source note | uspto-grants-2004_04 |
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