참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hexane | HCID 8058 | — |
| 반응물 | Tetrahydro-2-hydroxyfuran | HCID 93002 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 촉매 | Benzyltriphenylphosphonium chloride | HCID 70671 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 5-Phenylpent-4-enyl-1-ol | HCID 5371695 | — |
반응 단계
To a suspension of 4 g of benzyltriphenylphosphonium chloride in 20 ml of tetrahydrofuran was added 7.07 ml of 1.6M hexane solution of n-butyl lithium under cooling at 0° C. After stirring at room temperature for 30 minutes, 1 g of 2-hydroxytetrahydrofuran was added, followed by stirring at room temperature for 16 hours. Subsequently, after refluxing for 2 hours, insolubles were filtered off and the solvent was distilled off. The residue was purified by silica gel column chromatography (solvent: hexane-ethyl acetate=2:1) to give 2 g of (E)-5-phenyl-4-penten-1-ol as a colorless oily substance.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04886817 |
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| 출처 데이터셋 | uspto-grants-1989_12 |
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| ORD ID | ord-021a769ec5bf44a297e6ddea2e4655b7 |
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| 출처 메모 | uspto-grants-1989_12 |
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