Acetic Anhydride → HCID 15586530, 화합물
반응식
[F:1][C@:2]12[C@@H:19]([OH:20])[CH2:18][C@@:16]3([CH3:17])[C@@H:12]([CH2:13][CH:14]=[C:15]3[S:21]([CH3:23])=O)[C@@H:11]1[CH2:10][CH2:9][C:8]1[C@:3]2([CH3:25])[CH:4]=[CH:5][C:6](=[O:24])[CH:7]=1.[C:26]([O:29]C(=O)C)(=[O:28])[CH3:27]>>[C:26]([O:29][CH2:23][S:21][C:15]1[C@:16]2([CH2:18][C@H:19]([OH:20])[C@@:2]3([F:1])[C@@H:11]([CH2:10][CH2:9][C:8]4[C@:3]3([CH3:25])[CH:4]=[CH:5][C:6](=[O:24])[CH:7]=4)[C@@H:12]2[CH2:13][CH:14]=1)[CH3:17])(=[O:28])[CH3:27]참가 물질
반응 조건
- 온도
- 110 °C
실험 절차
A mixture of 1.5 g of 9-fluoro-11β-hydroxy-17-(methylsulfinyl)androsta-1,4,16-trien -3-one, 70 ml of acetic anhydride and 2 g of fused sodium acetate is heated at 110° C. under nitrogen for 2 hours. The acetic anhydride is partially removed by distillation under vacuum and the resulting slurry is diluted with 1:1 chloroform-water. The organic layer is separated, washed with diluted sodium bicarbonate solution, water, dried over anhydrous sodium sulfate and evaporated in vacuo. The residue is dissolved in 4:1 chloroform-hexane and chromatographed on a 40 g-silica gel column. Elution with 1:4 hexane-chloroform gives 940 mg of slightly impure material. Two crystallizations from acetone-hexane give 350 mg of the title compound, melting point 193°-194° C., with consistent spectral data.
후처리
- customThe acetic anhydride is partially removed by distillation under vacuum
- additionthe resulting slurry is diluted with 1:1 chloroform-water
- customThe organic layer is separated
- washwashed with diluted sodium bicarbonate solution, water
- dry with materialdried over anhydrous sodium sulfate
- customevaporated in vacuo
- dissolutionThe residue is dissolved in 4:1 chloroform-hexane
- customchromatographed on a 40 g-silica gel column
- washElution with 1:4 hexane-chloroform
- customgives 940 mg of slightly impure material
- customTwo crystallizations from acetone-hexane
출처 및 근거
- ORD 기록
- ord-1e7b2cce9feb448595080ac1588ab066
- 출처 데이터셋
- uspto-grants-1979_03
- 특허 번호
- US04146538
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