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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1032029생성일: 2026년 10월 26일

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/reaction/1032029

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 번호US04956482
출처 데이터셋uspto-grants-1990_09
ORD IDord-8f7441fe1ee14c1497a8aab338e52dc6
출처 메모uspto-grants-1990_09