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HRID 328209作成日:2026年10月26日

Hydrogen Peroxide → 3-Methoxy-1,3,5(10),15-estratetraen-17alpha-ol

https://huagongshe.com/reaction/328209

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-1,3,5(10)-estratrieneHCID 12576929—
反応物HCID 178528034HCID 178528034—
溶媒EthanolHCID 702—
生成物3-Methoxy-1,3,5(10),15-estratetraen-17alpha-olHCID 22796837—

反応条件

温度0 °C

反応手順

1.9 g. of diphenyldiselenide is dissolved in 100 ml. of absolute ethanol and combined at room temperature with 500 mg. of sodium borohydride. After decolorization of the yellow solution, 2.5 g. of 16α,17α-epoxy-3-methoxy-1,3,5(10)-estratriene [B. Schoenecker et al., Z.Chem [Chemical News] 10 (6), (1910)] is added thereto, and the mixture is heated for 27 hours under reflux. After cooling to 0° C., 6 ml. of 30% H2O2 is added dropwise thereto, and the solution is gradually warmed to 50° C. After 2 hours, the solution is poured into ice water. The thus-precipitated product is vacuum-filtered, washed with water, taken up in methylene chloride, and dried over sodium sulfate. After the crude product has been chromatographed on silica gel with 5 - 7.5% acetone/hexane, 1.1 g. of 3-methoxy-1,3,5(10),15-estratetraen-17α-ol is isolated as an oily product.

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-e0bfc620d4834f2c86ce4fb8e416b3b7
出典メモuspto-grants-1977_04