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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant5-Methoxyfuran-2-carbaldehydeHCID 6208—
ReactantSodium MethoxideHCID 10942334—
Reactant4-AcetylbenzamideHCID 11159497—
SolventDimethylformamideHCID 6228—
Product4-[(E)-3-(5-methoxy-furan-2-yl)-acryloyl]-benzamideHCID 67177299—

Reaction Conditions

Temperature45 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09138427B2
Source datasetuspto-grants-2015_09
ORD IDord-7d9150f7561b4fc5b55ea545e5c966a2
Source noteuspto-grants-2015_09