참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | m-Formylbenzonitrile | HCID 90670 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 촉매 | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 3-Ethenylbenzonitrile | HCID 220543 | 62.9% |
반응 단계
To a stirred suspension of methyltriphenylphosphonium bromide (75 g, 209.71 mmol) in dry THF (750 mL) at 0° C. under nitrogen was added dropwise n-BuLi (83 mL, 2.5 M in hexanes, 207.50 mmol). The mixture was warmed to room temperature. 3-Cyanobenzaldehyde (25 g, 190.65 mmol) was added as a solid in 5 g batches, and the mixture was stirred at room temperature overnight. The reaction was quenched in water, and the solvent was removed under vacuum. The residue was dissolved in the minimal amount of THF, and triphenylphosphine oxide was precipitated using ether. The solid was filtered through diatomaceous earth, and the filtrate was concentrated. Distillation by Kugelrhor at 90° C./33 Pa (0.25 mm Hg) gave the product as a colorless oil (15.5 g, 62%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06936611B2 |
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| 출처 데이터셋 | uspto-grants-2005_08 |
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| ORD ID | ord-6ff1bc1bdf374fc5a7ab44fc1302f615 |
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| 출처 메모 | uspto-grants-2005_08 |
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