Aluminium lithium hydride → [4-(1-{4-[2-(t-Butyldimethylsilanyloxy)-3,3-dimethylbutoxy]-3-methylphenyl}-1-ethylpropyl)-2-methylphenyl]methanol

HRID 502057ノート

反応式

HRID 502057 の反応式
[Si:1]([O:8][CH:9]([C:35]([CH3:38])([CH3:37])[CH3:36])[CH2:10][O:11][C:12]1[CH:17]=[CH:16][C:15]([C:18]([C:23]2[CH:32]=[CH:31][C:26]([C:27](OC)=[O:28])=[C:25]([CH3:33])[CH:24]=2)([CH2:21][CH3:22])[CH2:19][CH3:20])=[CH:14][C:13]=1[CH3:34])([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[Si:1]([O:8][CH:9]([C:35]([CH3:36])([CH3:37])[CH3:38])[CH2:10][O:11][C:12]1[CH:17]=[CH:16][C:15]([C:18]([C:23]2[CH:32]=[CH:31][C:26]([CH2:27][OH:28])=[C:25]([CH3:33])[CH:24]=2)([CH2:19][CH3:20])[CH2:21][CH3:22])=[CH:14][C:13]=1[CH3:34])([C:4]([CH3:5])([CH3:7])[CH3:6])([CH3:2])[CH3:3]

参加物

4

実験手順

To a 0° C. solution of the methyl 4-(1-{4-[2-(t-butyldimethylsilanyloxy)-3,3-dimethyl-butoxy]-3-methylphenyl}-1-ethylpropyl)-2-methyl-benzoate (4.37 g, 8.09 mmol) in THF (50 mL) is added LiAlH4 (0.31 g, 8.09 mmol). The reaction is stirred for 10 m and allowed to warm to RT overnight. The mixture is cooled to 0° C. and quenched successively with H2O (0.3 mL), 15% NaOH (0.3 mL) and H2O (0.9 mL). The mixture is stirred for 10 m, warmed to RT, stirred for 20 m, filtered through celite with EtOAc (100 mL) wash, and concentrated to give the title compound (4.14 g, 8.08 mmol, 99%).

後処理

  1. temperatureThe mixture is cooled to 0° C.
  2. customquenched successively with H2O (0.3 mL), 15% NaOH (0.3 mL) and H2O (0.9 mL)
  3. stirringThe mixture is stirred for 10 m
  4. temperaturewarmed to RT
  5. stirringstirred for 20 m
  6. filtrationfiltered through celite with EtOAc (100 mL)
  7. washwash
  8. concentrationconcentrated

出典と根拠

ORDレコード
ord-0c14f63de5394c69b53446d5621800b0
出典データセット
uspto-grants-2010_08
特許番号
US07772425B2

反応ノート

読み込み中…