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HRID 247539作成日:2026年10月24日

p-Toluenesulfonic acid → (8S,10R,13S,14S)-3-methoxy-10,13-dimethyl-1,2,7,8,12,14,15,16-octahydrocyclopenta[a]phenanthren-17-one

https://huagongshe.com/ja/reaction/247539

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物Trimethyl orthoformateHCID 9005—
反応物1,4-DioxaneHCID 31275—
反応物9-DehydroandrostenedioneHCID 239595—
溶媒PyridineHCID 1049—
生成物(8S,10R,13S,14S)-3-methoxy-10,13-dimethyl-1,2,7,8,12,14,15,16-octahydrocyclopenta[a]phenanthren-17-oneHCID 13037635—

反応手順

11.5 g of 4,9(11)-androstadiene-3,17-dione [U.S. Pat. No. 3,441,559 (1969)]in 200 ml of dioxane is reacted with 20 ml of orthoformic acid trimethyl ester and 100 mg of p-toluenesulfonic acid. After 48 hours, 5 ml of pyridine is added to the solution, the latter is concentrated under vacuum, the residue taken up in ethyl acetate, washed with water, and dried over sodium sulfate. After chromatography of the crude product with a hexane-ethyl acetate gradient on silica gel containing 2% triethylamine, 9.2 g of 3-methoxy-3,5,9(11)-androstatrien-17-one is isolated; mp 153.4° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04708823
出典データセットuspto-grants-1987_11
ORD IDord-9e421d8e61ef44e9b5e5876a0ec3ea0b
出典メモuspto-grants-1987_11