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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 894506생성일: 2026년 10월 26일

Sodium Fluoride → 3beta-Acetoxy-9alpha-fluoro-17alpha-hydroxy-16beta-methyl-5alpha-pregnan-20-one

https://huagongshe.com/reaction/894506

반응식

참여 물질

역할이름HCID투입량
반응물Sodium FluorideHCID 5235—
반응물Acetic AnhydrideHCID 7918—
반응물Sodium ThiosulfateHCID 24477—
반응물FluorineHCID 24524—
반응물Sodium TrifluoroacetateHCID 517019—
반응물3beta-Acetoxy-17alpha-hydroxy-16beta-methyl-5alpha-pregnan-20-oneHCID 70569590—
용매PyridineHCID 1049—
용매ChloroformHCID 6212—
용매TrichlorofluoromethaneHCID 6389—
생성물3beta-Acetoxy-9alpha-fluoro-17alpha-hydroxy-16beta-methyl-5alpha-pregnan-20-oneHCID 7057146350%

반응 단계

3β-Acetoxy-17α-hydroxy-16β-methyl-5α-pregnan-20-one (1 g, prepared by treatment of the corresponding 3β-ol with acetic anhydride in pyridine) was dissolved in fluorotrichloromethane (250 ml) and chloroform (200 ml) containing sodium trifluoroacetate (ca. 2 g) and sodium fluoride (ca. 2 g). The resulting solution was cooled to -78° and vigourously stirred, whereupon fluorine from four 750 cc bottles (8-10% v/v fluorine in nitrogen) was added over 9-10 hours. The reaction solution was then poured into aqueous sodium thiosulphate and the organic layer was separated, washed with water, dried over potassium carbonate and evaporated to dryness. The residue was purified by liquid chromatography, eluting with cyclohexane containing 30% v/v ethyl acetate and 0.1% v/v pyridine, to yield 3β-acetoxy-9α-fluoro-17α-hydroxy-16β-methyl-5α-pregnan-20-one (50%); m.p. 150° (after recrystallisation from acetone); PMR spectrum includes signals at δ2.20 (21-Me), 2.00 (3-O.CO.CH3), 0.92 (19-Me) and 0.87 (18-Me); FMR φ*+179.5 ppm. (Found: C, 70.51; H, 9.20; F, 4.48; C24H37FO4 requires C, 70.55; H, 9.18, F, 4.65%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04284558
출처 데이터셋uspto-grants-1981_08
ORD IDord-509bb40079154a639c1aa00b93809ced
출처 메모uspto-grants-1981_08