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HRID 328208作成日:2026年10月27日

Hydrogen Peroxide → (17beta)-13-Ethyl-3-methoxygona-1,3,5(10),15-tetraen-17-ol

https://huagongshe.com/reaction/328208

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen PeroxideHCID 784—
反応物Sodium borohydrideHCID 4311764—
反応物16alpha,17alpha-Epoxy-3-methoxy-18-methyl-1,3,5(10)-estratrieneHCID 86734624—
反応物HCID 178528034HCID 178528034—
溶媒EthanolHCID 702—
生成物(17beta)-13-Ethyl-3-methoxygona-1,3,5(10),15-tetraen-17-olHCID 86734623—

反応条件

温度0 °C

反応手順

3.7 g. of diphenyldiselenide is dissolved in 200 ml. of absolute ethanol and combined at room temperature with 1.0 g. of sodium borohydride. After the yellow solution has lost its color, 5.0 g. of 16α,17α-epoxy-3-methoxy-18 -methyl-1,3,5(10)-estratriene is added thereto and the mixture is heated under reflux for 30 hours. The solution is then cooled to 0° C. Dropwise, 11ml. of 30% H2O2 is added to the reaction solution and the latter is then gradually heated to 50° C. After 2 hours, the solution is introduced into ice water. The precipitate is vacuum-filtered, washed with water, and taken up in methylene chloride. After chromatography on silica gel with 6-8% acetone/hexane, 1.9 g. of 3-methoxy-18-methyl-1,3,5(10),15-estratetraen-17α-ol is obtained as an oily product. [α]D 20 = -108°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04016269
出典データセットuspto-grants-1977_04
ORD IDord-47443581362643fe9d5aadc35279fb3a
出典メモuspto-grants-1977_04