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Water → (R)-2-Phenylbutan-1-ol

HRID 636757
ノート
印刷プレビュー

反応式

HRID 636757 の反応式
[H-].[H-].[H-].[H-].[Li+].[Al+3].[C:7]1([C@@H:13]([CH2:17][CH3:18])[C:14](O)=[O:15])[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.O.[OH-].[K+]>C1COCC1>[C:7]1([C@@H:13]([CH2:17][CH3:18])[CH2:14][OH:15])[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962Water2 回HCID 14797Potassium HydroxideHCID 7853302-Phenylbutyric acid, (R)-HCID 21226445Aluminium lithium hydride

生成物 1

HCID 5325939(R)-2-Phenylbutan-1-ol

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート
温度
60 °C

実験手順

To a suspension of 2.3 gm of LAH (60.6 mmol) in 70 mL of THF was slowly added a solution of 5 gm of (R)-(−)-2-phenylbutyric acid (30.45 mmol, Aldrich) in 30 mL of THF. The reaction mixture was heated to 60° C. for 3 hr. The reaction was cooled to 0° C. and to it was successively added 2 mL of water, 2 mL of 1N KOH and 2 mL of water. The aluminum salts were removed by filtration and washed with 100 mL of ethylacetate. The filtrate was dried over MgSO4, filtered and concentrated to give the title compound which was used without purification.

後処理

  1. temperatureThe reaction was cooled to 0° C. and to it
  2. customThe aluminum salts were removed by filtration
  3. washwashed with 100 mL of ethylacetate
  4. dry with materialThe filtrate was dried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated

出典と根拠

ORDレコード
ord-b916815584f14b6080ddb315ae39c57b
出典データセット
uspto-grants-2001_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06194458B1

反応ノート

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