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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 567390생성일: 2026년 10월 24일

Bromoethene → 1,4-Pentadien-3-ol, 3-methyl-1-(2,6,6-trimethyl-1-cyclohexen-1-yl)-

https://huagongshe.com/ko/reaction/567390

반응식

참여 물질

역할이름HCID투입량
반응물BromoetheneHCID 11641—
반응물I2-IononeHCID 638014—
반응물MagnesiumHCID 5462224—
용매TetrahydrofuranHCID 8028—
생성물1,4-Pentadien-3-ol, 3-methyl-1-(2,6,6-trimethyl-1-cyclohexen-1-yl)-HCID 6436846837.1%

반응 조건

온도7.5 °C

반응 단계

0.1 mols of magnesium turnings are suspended in 50 ml of THF and treated with some drops of a solution of 0.12 mols of vinyl bromide in 100 ml of THF with stirring and under nitrogen atmosphere. As soon as the Grignard starts to form, the mixture is is cooled to 5-10° C. and added with the remaining solution of vinyl bromide in 30 min. The mixture is then cooled to −60° C. and added with 0.09 mols of beta ionone in 100 ml of THF in 20 min. The mixture is left to warm to room temperature, then heated at 40° C. for 2 hours. After that, the reaction is quenched as above described and vinyl beta-ionol is recovered by double distillation under vacuum, to obtain 166 g of a product, corresponding to an about 84% yield, with purity higher than 90%, determined by NMR.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06177579B1
출처 데이터셋uspto-grants-2001_01
ORD IDord-209895f0c3fa4b99a666bb710cc5c737
출처 메모uspto-grants-2001_01