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Water → (R)-2-Phenylbutan-1-ol

HRID 636757
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HRID 636757 반응식
[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
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962Water2회HCID 14797Potassium HydroxideHCID 7853302-Phenylbutyric acid, (R)-HCID 21226445Aluminium lithium hydride

생성물 1

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

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

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이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
온도
60 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-b916815584f14b6080ddb315ae39c57b
출처 데이터셋
uspto-grants-2001_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06194458B1

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