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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 280078생성일: 2026년 10월 26일

Silica → 17alpha-Acetyl-17beta-hydroxy-6,16-dimethyleneandrost-4-en-3-one

https://huagongshe.com/reaction/280078

반응식

참여 물질

역할이름HCID투입량
반응물SilicaHCID 24261—
반응물Sodium AcetateHCID 517045—
반응물17alpha-Ethynyl-17beta-hydroxy-6,16-dimethyleneandrosta-4-en-3-oneHCID 13314929—
용매WaterHCID 962—
생성물17alpha-Acetyl-17beta-hydroxy-6,16-dimethyleneandrost-4-en-3-oneHCID 13314931—

반응 조건

온도45 °C

반응 단계

9.0 Kg of 17α-ethynyl-17β-hydroxy-6,16-dimethyleneandrost-4-en-3-one is added to a reactor vessel, flushed with nitrogen until the oxygen content is less than 4%. 108 Liters (85.3 Kg) of acetone is added and the solution heated to 45° C. A catalyst solution (prepared by the addition of 0.72 liters conc. sulfuric acid to 10.8 liters of deionized water, followed by the addition of 576 grams of mercuric oxide, red powder to the dilute acid) is added to the reaction mixture and stirred at 45° C. until the reaction is complete, as monitored by TLC. The reaction mixture is cooled to less than 25° C. and 2.3 Kg Celite 545, 2.2 Kg sodium acetate and 20 liters of water added and mixture stirred for 15 min. The resulting crude product is filtered using a pot filter coated with Celite 545. The reactor is rinsed with 50 liters of acetone and filtered. The combined filtrate is concentrated under vacuum to about 50 liters, cooled to below 20° C. and stirred for 15 min. The slurry is filtered and the filter cake washed with 10 liters of acetone and 20 liters of water. The filter cake is dried in a vacuum oven at 50° C. to yield 17α-acetyl-17β-hydroxy-6,16-dimethyleneandrost-4-en-3-one (mercury content 10,500 ppm).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04588529
출처 데이터셋uspto-grants-1986_05
ORD IDord-788cffc4036c42ba988d443c58839c4b
출처 메모uspto-grants-1986_05