HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 611067Generated: November 1, 2026
Diethyl Ether → (E)-ethyl 3-(furan-3-yl)acrylate
https://huagongshe.com/reaction/611067
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 3-Furaldehyde | HCID 10351 | — |
| Reactant | Triethyl phosphonoacetate | HCID 13345 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | (E)-ethyl 3-(furan-3-yl)acrylate | HCID 10103508 | — |
Reaction Steps
To a solution of 17.7 g (78.8 mmol) of ethyl diethylphosphonoacetate in 150 ml of benzene, 2.89 g (72.2 mmol) of sodium hydride (60% in oil) was added under ice-cooling, followed by stirring for 30 minutes. To this solution, a solution of 6.308 g (65.65 mmol) of 3-furaldehyde in 50 ml of benzene was added dropwise, followed by stirring at room temperature for 30 minutes and refluxing for 30 minutes. After the reaction mixture was cooled to room temperature, ether was added; the mixture was then washed with water. The ether solution was dried over anhydrous magnesium sulfate; the solvent was distilled off under reduced pressure. The resulting crude product was purified by silica gel column chromatography (hexane to hexane/ethyl acetate=9/1) to yield the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05998433 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-afe5c1d3b79a4e8193a80a8094624352 |
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| Source note | uspto-grants-1999_12 |
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