돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 537723생성일: 2026년 10월 26일

Trifluoroacetic acid → 21-Hydroxy-17-(1-oxobutoxy)pregna-4,9(11)-diene-3,20-dione

https://huagongshe.com/reaction/537723

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물1,4-DioxaneHCID 31275—
반응물AnecortaveHCID 7074810—
용매1-Ethoxybutane-1,1-diolateHCID 86584763—
생성물21-Hydroxy-17-(1-oxobutoxy)pregna-4,9(11)-diene-3,20-dioneHCID 11704352—

반응 조건

온도45 °C

반응 단계

4 g (11.6 mM) of 17α,21-dihydroxy-pregna-4,9(11)-diene-3,20-dione were reacted with 20 mg of trifluoroacetic acid in 20 ml of dioxane and 10 ml of ethyl orthobutyrate for 5 hours at 100° C., and the low boiling head fraction was distilled off. The solution was cooled, then treated with 5 ml of a tartaric acid molar solution and heated to 40-50° C. for about 5 minutes to obtain 17α-butanoyloxy-21-hydroxy-pregna-4,9(11)-diene-3,20-dione. The solvent was evaporated off under vacuum and the residue was repeatedly taken up with dioxane. The resulting residue was dissolved in 200 ml of acetone and then 12 g trifluoroethyl octadecanoate (prepared from octadecanoyl chloride and trifluoroethanol), 20 g of Candida cylindracea lipase were added and the resulting suspension was stirred for 8-10 hours at 50° C., adding 2 g of C. cylindracea at regular time intervals. The lipase was filtered off, the filtrate was concentrated under vacuum and the residue was chromatographed on a silica gel column with a dichloromethane/methanol 98.5:1.5 mixture. The neat fraction was evaporated to obtain 4.9 g (7.17 mM) of 17α-butanoyloxy-21-octadecanoyloxy-pregna-4,9(11)-diene-3,20-dione.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08865690B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-0a4c70b37ee0403780735d55bd744536
출처 메모uspto-grants-2014_10