Aluminium lithium hydride → 19-Trimethylsiloxy-5alpha-androstane-3beta,17beta-diol
反応式
C([O:4][C@H:5]1[CH2:22][CH2:21][C@@:20]2([CH2:23][O:24][Si:25]([CH3:28])([CH3:27])[CH3:26])[C@@H:7]([CH2:8][CH2:9][C@@H:10]3[C@@H:19]2[CH2:18][CH2:17][C@@:15]2([CH3:16])[C@H:11]3[CH2:12][CH2:13][C@@H:14]2[O:29]C(=O)C)[CH2:6]1)(=O)C.[H-].[Al+3].[Li+].[H-].[H-].[H-]>CCOCC>[CH3:27][Si:25]([CH3:26])([CH3:28])[O:24][CH2:23][C@@:20]12[C@@H:19]3[C@H:10]([C@H:11]4[C@@:15]([CH2:17][CH2:18]3)([CH3:16])[C@@H:14]([OH:29])[CH2:13][CH2:12]4)[CH2:9][CH2:8][C@H:7]1[CH2:6][C@@H:5]([OH:4])[CH2:22][CH2:21]2参加物
4
実験手順
A solution of 19-trimethylsiloxy-5α-androstane-3β,17β-diol diacetate in ether is added to a lithium aluminum hydride suspension in ether. After refluxing for one hour, the excess hydride is destroyed with water. The ether solution is separated, dried over sodium sulfate and concentrated under vacuum. The residue which remains is crystallized from methanol to yield 19-trimethylsiloxy-5α-androstane-3β,17β-diol.