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HRID 894506作成日:2026年10月27日

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

https://huagongshe.com/reaction/894506

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium FluorideHCID 5235—
反応物Acetic AnhydrideHCID 7918—
反応物Sodium ThiosulfateHCID 24477—
反応物FluorineHCID 24524—
反応物Sodium TrifluoroacetateHCID 517019—
反応物3beta-Acetoxy-17alpha-hydroxy-16beta-methyl-5alpha-pregnan-20-oneHCID 70569590—
溶媒PyridineHCID 1049—
溶媒ChloroformHCID 6212—
溶媒TrichlorofluoromethaneHCID 6389—
生成物3beta-Acetoxy-9alpha-fluoro-17alpha-hydroxy-16beta-methyl-5alpha-pregnan-20-oneHCID 7057146350%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04284558
出典データセットuspto-grants-1981_08
ORD IDord-509bb40079154a639c1aa00b93809ced
出典メモuspto-grants-1981_08