HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066964Generated: October 30, 2026
Acetic Acid → Methyl 2-{(benzofuran-5-yl)methylene}-3-oxobutyrate
https://huagongshe.com/reaction/1066964
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 (0.6 g, 4.1 mmol), methyl acetoacetate (0.52 g, 4.5 mmol), piperidine (0.019 g, 0.225 mmol), and acetic acid (0.014 g, 0.225 mmol) in benzene (30 mL) was stirred and refluxed with a Dean-Stark trap for 8 h. Benzene was evaporated, 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 in sequence. The ethyl acetate solution was dried (magnesium sulfate), solvent removed under reduced pressure and the residue was purified by column chromatography (SiO2, EtOAc/hexane, 10%-15%). The product, methyl 2-{(benzofuran-5-yl)methylene}-3-oxobutyrate, was obtained as an oil (0.98 g, 98.3%) 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 | US06245773B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-4119453516d0493384c98ee6e4b75079 |
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| Source note | uspto-grants-2001_06 |
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