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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 247539생성일: 2026년 10월 24일

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/ko/reaction/247539

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물Trimethyl orthoformateHCID 9005—
반응물1,4-DioxaneHCID 31275—
반응물9-DehydroandrostenedioneHCID 239595—
용매PyridineHCID 1049—
생성물(8S,10R,13S,14S)-3-methoxy-10,13-dimethyl-1,2,7,8,12,14,15,16-octahydrocyclopenta[a]phenanthren-17-oneHCID 13037635—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04708823
출처 데이터셋uspto-grants-1987_11
ORD IDord-9e421d8e61ef44e9b5e5876a0ec3ea0b
출처 메모uspto-grants-1987_11