Aluminium lithium hydride → (S)-2-((1R,3aR,4S,7aR)-4-((tert-butyldimethylsilyl)oxy)-7a-methyloctahydro-1H-inden-1-yl)propan-1-ol

HRID 388732

反応式

HRID 388732 の反応式
C([O:7][CH2:8][C@H:9]([C@@H:11]1[C@:19]2([CH3:20])[C@H:14]([C@@H:15]([O:21][Si:22]([C:25]([CH3:28])([CH3:27])[CH3:26])([CH3:24])[CH3:23])[CH2:16][CH2:17][CH2:18]2)[CH2:13][CH2:12]1)[CH3:10])(=O)C(C)(C)C.[H-].[Al+3].[Li+].[H-].[H-].[H-]>CCOCC>[Si:22]([O:21][C@H:15]1[CH2:16][CH2:17][CH2:18][C@@:19]2([CH3:20])[C@H:14]1[CH2:13][CH2:12][C@@H:11]2[C@H:9]([CH3:10])[CH2:8][OH:7])([C:25]([CH3:28])([CH3:27])[CH3:26])([CH3:24])[CH3:23]

参加物

4

反応物 2

HCID 21226445Aluminium lithium hydrideHCID 68939165HCID 68939165、化合物

生成物 1

HCID 15230899(S)-2-((1R,3aR,4S,7aR)-4-((tert-butyldimethylsilyl)oxy)-7a-methyloctahydro-1H-inden-1-yl)propan-1-ol

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒2 回

反応条件

温度
-30 °C

実験手順

The compound of Example 10D (6.45 g, 16 mmol) was dissolved in 30 mL of ether and cooled to −30° C.; 35 mL of a 1 N solution of lithium aluminum hydride in ether was added at a rate so as to maintain a constant temperature and a modest rate of gas evolution. The mixture was stirred at −30° C. for 10 minutes, and then it was warmed to 0° C. for 1 hour. The reaction was quenched by the careful addition of ethyl acetate (Caution! Vigorous gas evolution) and stirred for 10 minutes, then quenched with a solution of Rochelle's salt. The resultant mixture was partitioned between ethyl acetate and water; the organic phase was washed with brine and dried over Na2SO4. The solvents were removed in vacuo, and the residue was purified by chromatography on an Analogix Intelliflash 280™, eluting with a gradient of 5% to 30% ethyl acetate in hexanes.

後処理

  1. temperatureto maintain a constant temperature
  2. temperatureit was warmed to 0° C. for 1 hour
  3. customThe reaction was quenched by the careful addition of ethyl acetate (Caution! Vigorous gas evolution)
  4. stirringstirred for 10 minutes
  5. customquenched with a solution of Rochelle's salt
  6. customThe resultant mixture was partitioned between ethyl acetate and water
  7. washthe organic phase was washed with brine
  8. dry with materialdried over Na2SO4
  9. customThe solvents were removed in vacuo
  10. customthe residue was purified by chromatography on an Analogix Intelliflash 280™
  11. washeluting with a gradient of 5% to 30% ethyl acetate in hexanes

出典と根拠

ORDレコード
ord-145e01aa6f0d430e94077d7accf22106
出典データセット
uspto-grants-2013_02
特許番号
US08377913B2

関連ノート

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