Cerium(III) chloride → 17alpha-Ethinyl-11beta-fluoro-17beta-hydroxy-7alpha-methylestr-4-en-3-one
反応式
[Cl-].[Ce+3].[Cl-].[Cl-].[C:5]([Mg]Br)#[CH:6].[F:9][C@H:10]1[CH2:27][C@@:25]2([CH3:26])[C@@H:21]([CH2:22][CH2:23][C:24]2=[O:28])[C@H:20]2[C@H:11]1[C@@H:12]1[C:17](=[CH:18][C@H:19]2[CH3:29])[CH:16]=[C:15]([O:30]C)[CH2:14][CH2:13]1.[Cl-].[NH4+]>O1CCCC1.O>[C:5]([C@:24]1([OH:28])[CH2:23][CH2:22][C@H:21]2[C@H:20]3[C@H:11]([C@@H:10]([F:9])[CH2:27][C@:25]12[CH3:26])[C@@H:12]1[C:17](=[CH:16][C:15](=[O:30])[CH2:14][CH2:13]1)[CH2:18][C@H:19]3[CH3:29])#[CH:6]参加物
反応物 4
生成物 1
試薬・触媒・溶媒 2
反応条件
- 温度
- 0 °C
実験手順
A solution of 9.17 g of cerium(III) chloride in 60 ml of tetrahydrofuran was mixed drop by drop at 0° C. with 74.2 ml of an ethinylmagnesium bromide solution (0.5 M in tetrahydrofuran) and stirred for 1 hour at 0° C. Then, a solution of 2 g of crude 11β-fluoro-3-methoxy-7α-methylestra-3,5-dien-17-one in 40 ml of tetrahydrofuran was added drop by drop and stirred for another 3.5 hours at 0° C. For working-up, a saturated ammonium chloride solution was added, added to water, extracted three times with ethyl acetate, washed with semiconcentrated hydrochloric acid, sodium bicarbonate solution and sodium chloride solution, dried on sodium sulfate, concentrated by evaporation in a vacuum and chromatographed on silica gel with hexane/ethyl acetate. 1.15 g of pure 17α-ethinyl-11β-fluoro-17β-hydroxy-7α-methylestr-4-en-3-one with a melting point of 218-220° C. was obtained. [α]D=+19.2° (CHCl3).
後処理
- stirringstirred for another 3.5 hours at 0° C
- extractionextracted three times with ethyl acetate
- washwashed with semiconcentrated hydrochloric acid, sodium bicarbonate solution and sodium chloride solution
- customdried on sodium sulfate
- concentrationconcentrated by evaporation in a vacuum
- customchromatographed on silica gel with hexane/ethyl acetate
出典と根拠
- ORDレコード
- ord-a068e470c15640649308e82e389c95f1
- 出典データセット
- uspto-grants-2007_08
- 特許番号
- US07262023B2
反応ノート
読み込み中…