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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37305생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/37305

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, 5H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05420153
출처 데이터셋uspto-grants-1995_05
ORD IDord-3a39a55380c9432ea51b387bb28c73e5
출처 메모uspto-grants-1995_05