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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 53996생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물4-(Hydroxymethyl)benzaldehydeHCID 556330—
반응물(5-Cyano-2-benzofuranyl)methyltriphenylphosphonium chlorideHCID 21844326—
용매EthanolHCID 702—
용매TetrahydrofuranHCID 8028—
생성물2-[2-(4-Hydroxymethylphenyl)vinyl]-5-benzofurancarbonitrileHCID 54093245189.6%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05620991
출처 데이터셋uspto-grants-1997_04
ORD IDord-8adc7a61c8d94ae6acdb753736bae13d
출처 메모uspto-grants-1997_04