Tetrahydrofuran → Estra-1,3,5(10),16-tetraen-3,6-diol
反応式
[H-].[Al+3].[Li+].[H-].[H-].[H-].[CH3:7][C@:8]12[CH2:24][CH2:23][C@H:22]3[C@@H:13]([CH2:14][C:15](=[O:29])[C:16]4[CH:17]=[C:18](CC([O-])=O)[CH:19]=[CH:20][C:21]=43)[C@@H:12]1[CH2:11][CH:10]=[CH:9]2.C1C[O:33]CC1>>[CH3:7][C@:8]12[CH2:24][CH2:23][C@H:22]3[C@@H:13]([CH2:14][CH:15]([OH:29])[C:16]4[CH:17]=[C:18]([OH:33])[CH:19]=[CH:20][C:21]=43)[C@@H:12]1[CH2:11][CH:10]=[CH:9]2参加物
実験手順
To a suspension of lithium aluminum hydride (LAH, 95%, 46.9 mg, 1.17 mmol) in 5 mL of anhydrous THF was added estra-1,3,5(10),16-tetraen-6-one-3-yl-acetate (6) (422.9 mg, 1.360 mmol) in 5 mL of anhydrous THF dropwise, with stirring. The reaction was stirred 50 min., after which further LAH (46.5 mg, 1.16 mmol) was added and the reaction stirred 22 h. After refluxing 4 h TLC still showed starting material. The reaction was quenched with 0.5 mL of water+0.5 mL of 20% (w/w) sulfuric acid and concentrated under reduced pressure. The residue was extracted four times with 10 mL portions of hot ethyl acetate and filtered through Celite. The combined filtrates were concentrated and purified twice by flash chromatography to give solid product (0.05 g, 0.2 mmol, 10%), m.p. 150-157° C.
後処理
- stirringThe reaction was stirred 50 min.
- stirringthe reaction stirred 22 h
- temperatureAfter refluxing 4 h TLC
- customThe reaction was quenched with 0.5 mL of water+0.5 mL of 20% (w/w) sulfuric acid
- concentrationconcentrated under reduced pressure
- extractionThe residue was extracted four times with 10 mL portions of hot ethyl acetate
- filtrationfiltered through Celite
- concentrationThe combined filtrates were concentrated
- custompurified twice by flash chromatography
出典と根拠
- ORDレコード
- ord-299a6fe9d7414c8e97b7b4bf472d5c09
- 出典データセット
- uspto-grants-2000_10
- 特許番号
- US06140316
反応ノート
読み込み中…