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HRID 128779생성일: 2026년 10월 23일

18-Crown-6 → 1-(2-Methoxyethenyl)-4-(octyloxy)benzene

https://huagongshe.com/ko/reaction/128779

반응식

참여 물질

역할이름HCID투입량
반응물18-Crown-6HCID 28557—
반응물p-(Octyloxy)benzaldehydeHCID 90358—
반응물Methoxymethyl-triphenylphosphonium chlorideHCID 2723798—
반응물Potassium tert-butoxideHCID 23665647—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물1-(2-Methoxyethenyl)-4-(octyloxy)benzeneHCID 53775512—

반응 단계

Potassium t-butoxide (1.9 g) is added to a slurry of methoxymethyl triphenylphosphonium chloride (6.17 g) and 18-Crown-6 (100 mg) in dry THF (40 ml). The mixture is stirred for 5 min, cooled to 15°, and a solution of 4-octyloxybenzaldehyde (3.52 g) in THF (5 ml) is added dropwise. The reaction mixture is stirred at room temperature for 20 min, diluted with 250 ml hexane, and the resulting mixture filtered through a pad of diatomaceous earth. Evaporation of the filtrate leaves crude 1-(2-methoxyethenyl)-4-(octyloxy)benzene as a mixture of cis and trans isomers, containing about 15 mol % triphenylphosphine oxide. The crude material may be used as is, or may be chromatographed with 1:1 hexanedichloromethane.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05464865
출처 데이터셋uspto-grants-1995_11
ORD IDord-342bcfb170dd446095d890ba2b2078d3
출처 메모uspto-grants-1995_11