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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1087671생성일: 2026년 10월 25일

Water → 9-Dehydroandrostenedione

https://huagongshe.com/reaction/1087671

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Chlorosulfonic acidHCID 24638—
반응물9alpha-Hydroxyandrost-4-ene-3,17-dioneHCID 10425017—
용매DichloromethaneHCID 6344—
생성물9-DehydroandrostenedioneHCID 239595—

반응 단계

9α-Hydroxyandrostenedione (10.00 g.) is dissolved in methylene chloride (100 ml.) and cooled to 0°-5°. Chlorosulfonic acid (5 ml.) is added dropwise and the mixture stirred to 0.5 hour at 0°-5°. Water (50 ml.) is added dropwise while the temperature rises to 23°. The mixture is stirred for 5 minutes and the phases separated. The organic phase is washed with an aqueous sodium bicarbonate solution (10%, 25 ml.) and water (50 ml.) containing 10 ml. of a saturated sodium chloride solution. Each of the aqueous washes is back extracted with the same methylene chloride (25 ml.) which is then added to the organic phase. The organic phase is concentrated to approximately 50 ml. Heptane (100 ml.) is added and the mixture concentrated to approximately 50 ml. with the temperature reaching a maximum of about 35°. The mixture is cooled to 0°-5°, Stirred 0.5 hour, the solids are collected by filtration, under vacuum at 55° to give androsta-4,9(11)-diene-3,17-dione, 8.95 g. (89.5% weight yield, 95.0% chemical yield). GC (Example 1) shows 99% androsta-4,9(11)-diene-3,17-dione.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE033364
출처 데이터셋uspto-grants-1990_10
ORD IDord-d14822fcf9cf4973aa1bcfea28061c40
출처 메모uspto-grants-1990_10