Acetic Acid → 7a-(5-Hydroxypentyl)-estr-4-ene-3,17-dione
反応式
[Si]([O:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][C@@H:14]1[CH2:31][C:30]2[C@H:25]([CH2:26][CH2:27][C:28](=[O:32])[CH:29]=2)[C@@H:24]2[C@@H:15]1[C@H:16]1[C@@:20]([CH2:22][CH2:23]2)([CH3:21])[C:19](=[O:33])[CH2:18][CH2:17]1)(C(C)(C)C)(C)C.C(O)(=O)C>CO.O>[OH:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][C@@H:14]1[CH2:31][C:30]2[C@H:25]([CH2:26][CH2:27][C:28](=[O:32])[CH:29]=2)[C@@H:24]2[C@@H:15]1[C@H:16]1[C@@:20]([CH2:22][CH2:23]2)([CH3:21])[C:19](=[O:33])[CH2:18][CH2:17]1参加物
5
実験手順
A solution of 125.4 g of 7α-(5-tert-butyldimethylsilyloxypentyl)-estr-4-ene-3,17-dione in 625 ml of methanol and 347 ml of water is stirred with 694 ml of glacial acetic acid for 2.5 hours at 50° C. After the concentration by evaporation at 60° C. in a vacuum, 94.1 g of crude 7α-(5-hydroxypentyl)-estr-4-ene-3,17-dione is obtained as oil.