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HRID 53996作成日:2026年10月26日

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

https://huagongshe.com/reaction/53996

反応式

関与物質

役割名称HCID仕込み量
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物4-(Hydroxymethyl)benzaldehydeHCID 556330—
反応物(5-Cyano-2-benzofuranyl)methyltriphenylphosphonium chlorideHCID 21844326—
溶媒EthanolHCID 702—
溶媒TetrahydrofuranHCID 8028—
生成物2-[2-(4-Hydroxymethylphenyl)vinyl]-5-benzofurancarbonitrileHCID 54093245189.6%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05620991
出典データセットuspto-grants-1997_04
ORD IDord-8adc7a61c8d94ae6acdb753736bae13d
出典メモuspto-grants-1997_04