Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1901363생성일: 2026년 10월 25일
1,8-Diazabicyclo(5.4.0)undec-7-ene → 2-[2-(4-Hydroxymethylphenyl)vinyl]-5-benzofurancarbonitrile
https://huagongshe.com/reaction/1901363
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| 반응물 | 4-(Hydroxymethyl)benzaldehyde | HCID 556330 | — |
| 반응물 | (5-Cyano-2-benzofuranyl)methyltriphenylphosphonium chloride | HCID 21844326 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-[2-(4-Hydroxymethylphenyl)vinyl]-5-benzofurancarbonitrile | HCID 54093245 | 189.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05576343 |
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| 출처 데이터셋 | uspto-grants-1996_11 |
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| ORD ID | ord-b1b1035320d943f5a0038318f06c0b46 |
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| 출처 메모 | uspto-grants-1996_11 |
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