Sodium borohydride → 2(S)-t-Butyldimethylsilyloxy-2-phenylethanol

HRID 1682741ノート

反応式

HRID 1682741 の反応式
[BH4-].[Na+].[Si:3]([O:10][C@@H:11]([C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)[C:12](OCC)=[O:13])([C:6]([CH3:9])([CH3:8])[CH3:7])([CH3:5])[CH3:4]>CO>[Si:3]([O:10][C@@H:11]([C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1)[CH2:12][OH:13])([C:6]([CH3:9])([CH3:8])[CH3:7])([CH3:5])[CH3:4]

参加物

4

反応物 2

HCID 4311764Sodium borohydride2 回HCID 10968419ethyl (S)-alpha-(t-butyldimethylsilyloxy)-alpha-phenylacetate

生成物 1

HCID 228670812(S)-t-Butyldimethylsilyloxy-2-phenylethanol

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

15.5 g of sodium borohydride were added in portions, whilst ice-cooling, to a solution of 20 g of ethyl (S)-α-t-butyldimethylsilyloxy-α-phenylacetate [prepared as described in step (a) above] in 500 ml of absolute methanol, and the resulting mixture was stirred overnight at room temperature. At the end of this time, 10 g of sodium borohydride were added in portions, whilst ice-cooling. The reaction mixture was then stirred at room temperature for 5 hours, after which it was concentrated by evaporation under reduced pressure, and the concentrate was mixed with water and ethyl acetate. The ethyl acetate layer was separated, washed with water and dried over anhydrous sodium sulfate, and then the solvent was removed by distillation under reduced pressure, to give the title compound as a crude product.

後処理

  1. temperaturecooling
  2. stirringThe reaction mixture was then stirred at room temperature for 5 hours
  3. concentrationafter which it was concentrated by evaporation under reduced pressure
  4. additionthe concentrate was mixed with water and ethyl acetate
  5. customThe ethyl acetate layer was separated
  6. washwashed with water
  7. dry with materialdried over anhydrous sodium sulfate
  8. customthe solvent was removed by distillation under reduced pressure

出典と根拠

ORDレコード
ord-a5b7f5b8d1db4817a34e55de5a6fbaa2
出典データセット
uspto-grants-1997_06
特許番号
US05635534

反応ノート

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