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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 129532생성일: 2026년 10월 26일

Cyclododecanecarboxaldehyde → 1-(3-Phenyl-1-propenyl)cyclododecane

https://huagongshe.com/reaction/129532

반응식

참여 물질

역할이름HCID투입량
반응물CyclododecanecarboxaldehydeHCID 78737—
반응물Phenethyltriphenylphosphonium bromideHCID 10863251—
반응물ButyllithiumHCID 178418339—
용매Diethyl EtherHCID 3283—
생성물1-(3-Phenyl-1-propenyl)cyclododecaneHCID 5447171688.2%

반응 조건

온도0 °C

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, 5

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05468774
출처 데이터셋uspto-grants-1995_11
ORD IDord-c1a0464607584b3bbe40ecd0acae5021
출처 메모uspto-grants-1995_11