HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2280270Generated: October 27, 2026
Methanol → 4-[(E)-3-(5-methoxy-furan-2-yl)-acryloyl]-benzamide
https://huagongshe.com/reaction/2280270
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 5-Methoxyfuran-2-carbaldehyde | HCID 6208 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 4-Acetylbenzamide | HCID 11159497 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-[(E)-3-(5-methoxy-furan-2-yl)-acryloyl]-benzamide | HCID 67177299 | — |
Reaction Steps
Sodium methoxide (in portions) was added, over a time interval of about three minutes, to 4-acetyl-benzamide (1.38 g, 8.5 mmol) and 5-methoxy-furan-2-carbaldehyde (1.31 g, 10.6 mmol) in a 1:1 mixture of methanol and dimethylformamide (16 mL). The resulting solution was placed under N2 and stirred overnight at 45° C. The reaction mixture was then evaporated to dryness under vacuum, followed by the addition of water and brine (100 mL) to the resulting residue. The aqueous solution was extracted with ethyl acetate (125 mL×3) and the combined organic layers were washed with brine (100 mL) and dried over MgSO4. The crude reaction mixture of 4-[(E)-3-(5-methoxy-furan-2-yl)-acryloyl]-benzamide and unreacted 4-acetyl acetamide is used without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09138427B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-7d9150f7561b4fc5b55ea545e5c966a2 |
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| Source note | uspto-grants-2015_09 |
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