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HRID 3984作成日:2026年10月23日

Isopropenyl acetate → Cholesta-1,5,7-trien-3-ol

https://huagongshe.com/ja/reaction/3984

反応式

関与物質

役割名称HCID仕込み量
反応物Isopropenyl acetateHCID 7916—
反応物1,4,6-Cholestatrien-3-oneHCID 107390—
反応物Sodium borohydrideHCID 4311764—
反応物Calcium ChlorideHCID 5284359—
溶媒Acetic AcidHCID 176—
溶媒EthanolHCID 702—
溶媒MethanolHCID 887—
生成物Cholesta-1,5,7-trien-3-olHCID 1861155363%

反応条件

温度0 °C

反応手順

To a mixture of 38 g (0.1 mol) of cholesta-1,4,6-trien-3-one and 17 g (0.1 mol) of paratoluenesulfonic acid were added 400 g (4 mol) of isopropenyl acetate, and the mixture was heated under reflux for 3 hours. The reaction solution was thoroughly washed with water until it was neutral, and dried over sodium sulfate A solution of the thus obtained concentrate in 600 ml of ether was added dropwise at a temperature of -5° C. to -10° C. to a reducer solution and stirred at 0° C. for 6 hours, said reducer solution being prepared by cooling a solution of 90 g of calcium chloride in 1,500 ml of methanol to a temperature of -5° C. to -10° C., then adding dropwise thereto a solution of 45 g of sodium borohydride in 2,000 ml of ethanol, and stirring the reaction solution at a temperature of -5° C. to -10° C. for 60 minutes. After completion of the reaction, 50% acetic acid was added to the reaction mixture and the resultant solution was extracted with ether. The ethereal layer separated was washed with water and then sodium bicarbonate solution, dried over sodium sulfate and distilled under reduced pressure to remove ether therefrom. The residue was recrystallized from acetone to yield 23.9 g of cholesta-1,5,7-trien-3-ol (IV), m.p. 126°-127° C. The yield was 63%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04723045
出典データセットuspto-grants-1988_02
ORD IDord-0ef1704cd51e4103bf0c70a5c34931c8
出典メモuspto-grants-1988_02