Sulfuric Acid → HCID 9943709、化合物
反応式
S(=O)(=O)(O)O.O[C@@:7]12[C@@H:24]3[C@H:15]([C@H:16]4[C@@:20]([CH2:22][CH2:23]3)([CH3:21])[C:19](=[O:25])[CH2:18][CH2:17]4)[C@H:14]([CH3:26])[CH2:13][C:12]1=[CH:11][C:10](=[O:27])[CH2:9][CH2:8]2.C(OCC)(=O)C.CCCCCC>C(Cl)Cl>[CH3:26][C@@H:14]1[CH2:13][C:12]2[C:7]([CH2:8][CH2:9][C:10](=[O:27])[CH:11]=2)=[C:24]2[C@@H:15]1[C@H:16]1[C@@:20]([CH2:22][CH2:23]2)([CH3:21])[C:19](=[O:25])[CH2:18][CH2:17]1参加物
実験手順
To 15 ml of concentrated sulfuric acid (98%) cooled to ˜5° C. was added dropwise ˜20 Mm of a mixture containing 10-hydroxy-7α-methyl-estra-4-ene-3,17-dione (III) and 5,10-dihydroxy-7α-methyl-estra-3,17-dione (IV) from example 2 dissolved in 15 ml of methylene chloride. About 20 minutes after the addition was complete, TLC ({fraction (1/1)} ethyl acetate/hexane, Rf 0.4) showed that the reaction was complete. The deep red reaction mixture was poured over ice, washed in with methylene chloride, partially neutralized with potassium carbonate, and the phases separated. The organic phase was washed with dilute aqueous potassium carbonate, brine, and dried over sodium sulfate, and concentrated under vacuum to a solid product. This material was column chromatographed on 150 g of silica gel with gradient elution from ⅓ to {fraction (1/1)} ethyl acetate/hexane. Fractions 6-9 were combined to give a solid which was recrystallized from ethyl acetate to provide the title product. Mp 208-209° C.
後処理
- additionwas added dropwise ˜20 Mm of a mixture
- additionAbout 20 minutes after the addition
- customThe deep red reaction mixture
- additionwas poured over ice
- washwashed in with methylene chloride
- customthe phases separated
- washThe organic phase was washed with dilute aqueous potassium carbonate, brine
- dry with materialdried over sodium sulfate
- concentrationconcentrated under vacuum to a solid product
- customchromatographed on 150 g of silica gel with gradient elution from ⅓
- customto give a solid which
- customwas recrystallized from ethyl acetate
出典と根拠
- ORDレコード
- ord-641fa7084ebe48b2bcdb6335dab7071b
- 出典データセット
- uspto-grants-2004_11
- 特許番号
- US06812358B2
反応ノート
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