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HRID 2397524생성일: 2026년 10월 25일

Carbon Dioxide → Cholesta-1,5,7-trien-3-on-25-ol

https://huagongshe.com/reaction/2397524

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물PotassiumHCID 5462222—
반응물25-Hydroxycholesta-1,4,6-trien-3-oneHCID 22797387—
반응물Potassium tert-butoxideHCID 23665647—
용매1-ButanolHCID 263—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물Cholesta-1,5,7-trien-3-on-25-olHCID 22797385—

반응 단계

A reaction vessel was charged with 125 ml of dry dimethylsulfoxide and 2.5 g of cholesta-1,4,6-trien-3-on-25-ol was suspended in the dimethylsulfoxide. The suspension was heated, and 10 ml of dry ether was added to the resulting milky suspension to obtain a transparent solution. The reaction vessel was filled with dry argon gas. Powdery potassium t-butoxide prepared from 1.25 g potassium and 50 ml of butanol was added at one time to the solution under ice cooling and with violent agitation. The reaction mixture liquid was violently agitated for 12 minutes and was then poured into ice water saturated with carbon dioxide gas, which was prepared by adding dry ice to water. The mixture was then extracted with 600 ml of ether cooled to 0° to 5° C. The extract was promptly washed with cooled water saturated with a large quantity of carbon dioxide until the washing liquid became neutral, and the ether was then distilled off to obtain crude cholesta-1,5,7-trien-3-on-25-ol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04022768
출처 데이터셋uspto-grants-1977_05
ORD IDord-88a9042828054b91b46d372a7215c06f
출처 메모uspto-grants-1977_05