참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Cyclododecanecarboxaldehyde | HCID 78737 | — |
| 반응물 | Phenethyltriphenylphosphonium bromide | HCID 10863251 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | 1-(3-Phenyl-1-propenyl)cyclododecane | HCID 54471716 | 88.2% |
반응 단계
To 11.4 g (25.5 mmol) of phenylethyl triphenylphosphonium bromide in 50 mL of dry ether at 0° C. is added 10.2 mL (25.5 mmol) of 2.5M butyllithium. The suspension is stirred at 0° C. for 1 hour followed by the addition of 5.0 g (25.5 mmol) of cyclododecane carboxaldehyde. The mixture is stirred at room temperature for 3 hours after which time no starting material is evident by TLC. The reaction mixture is quenched with 1N HCl. The layers are separated and the aqueous layer is washed twice with ethyl ether. The combined organic layers are dried over a MgSO4 and the ether is evaporated. The residue is flash chromatographed on silica gel using hexanes to give 6.4 g of a colorless oil: NMR (CDCl3) δ 1.0-1.6 (m, 10H), 2.6 (m, 1H), 3.4 (d, 2H, J=8 Hz, ), 5.3 (t, 1H, J=7 Hz), 5.45 (q, 1H, J=7 Hz), 7.2 ppm (m, 5H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05420153 |
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| 출처 데이터셋 | uspto-grants-1995_05 |
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| ORD ID | ord-3a39a55380c9432ea51b387bb28c73e5 |
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| 출처 메모 | uspto-grants-1995_05 |
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