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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 53996Erstellt: 24. Oktober 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → 2-[2-(4-Hydroxymethylphenyl)vinyl]-5-benzofurancarbonitrile

https://huagongshe.com/de/reaction/53996

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Edukt4-(Hydroxymethyl)benzaldehydeHCID 556330—
Edukt(5-Cyano-2-benzofuranyl)methyltriphenylphosphonium chlorideHCID 21844326—
LösungsmittelEthanolHCID 702—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-[2-(4-Hydroxymethylphenyl)vinyl]-5-benzofurancarbonitrileHCID 54093245189,6%

Reaktionsschritte

911 mg of 4-hydroxymethylbenzaldehyde and 2.0 g of (5-cyano-2-benzofuranyl)methyltriphenylphosphonium chloride were dissolved in a solvent mixture of 10 ml of tetrahydrofuran and 10 ml of ethanol, followed by the addition of 845 mg of 1,8-diazabicyclo[5.4.0]-7-undecene and by subsequent stirring at room temperature for 1 hour. After distilling off the solvent, the resulting residue was purified by subjecting it to silica gel column chromatography, thereby obtaining 2.3 g of 2-[2-(4-hydroxymethylphenyl)vinyl]-5-benzofurancarbonitrile as a mixture of E and Z forms. 2.3 g of the thus obtained E/Z mixture was dissolved in a solvent mixture of 10 ml of tetrahydrofuran and 10 ml of ethanol, and the solution was subjected to catalytic hydrogenation under normal pressure for 7 hours in the presence of 800 mg of palladium oxide.1H2O.barium sulfate. After removing the catalyst by filtration and distilling off the solvent, the resulting residue was purified by subjecting it to silica gel column chromatography using chloroform as an elution solvent to obtain 835 mg of 2-[2-(4-hydroxymethylphenyl)ethyl]-5-benzofurancarbonitrile as crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05620991
Quelldatensatzuspto-grants-1997_04
ORD IDord-8adc7a61c8d94ae6acdb753736bae13d
Quellennotizuspto-grants-1997_04