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Water → 3-(2-Propoxyphenyl)-1-propanol

HRID 1169488
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HRID 1169488 반응식
[H-].[Al+3].[Li+].[H-].[H-].[H-].[CH2:7]([O:10][C:11]1[CH:23]=[CH:22][CH:21]=[CH:20][C:12]=1[CH:13]=[CH:14][C:15](OCC)=[O:16])[CH2:8][CH3:9].O.[OH-].[Na+]>C(OCC)C>[CH2:7]([O:10][C:11]1[CH:23]=[CH:22][CH:21]=[CH:20][C:12]=1[CH2:13][CH2:14][CH2:15][OH:16])[CH2:8][CH3:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962Water2회HCID 14798Sodium HydroxideHCID 21226445Aluminium lithium hydrideHCID 70025127Ethyl 2-propoxycinnamate

생성물 1

HCID 229900333-(2-Propoxyphenyl)-1-propanol수율 96.8%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매3회

실험 절차

To lithium aluminum hydride (6.87 g) suspended in diethyl ether (300 ml) was added dropwise at 0° C. a solution of ethyl 2-propoxycinnamate (21.2 g) in diethyl ether (100 ml) over a period of 40 minutes. After the dropwise addition, the resulting mixture was stirred at room temperature for one hour. Water (7 ml), a 15% aqueous solution of sodium hydroxide (7 ml) and water (21 ml) were added to the reaction mixture, and the resulting mixture was further stirred at room temperature for one hour. The reaction mixture was diluted with diethyl ether and was dried by addition of anhydrous magnesium sulfate. After the resulting mixture was filtered, the filtrate was concentrated under reduced pressure to obtain 3-(2-propoxyphenyl)-1-propanol (17.01 g) as a colorless oil.

후처리

  1. additionAfter the dropwise addition
  2. stirringthe resulting mixture was further stirred at room temperature for one hour
  3. dry with materialwas dried by addition of anhydrous magnesium sulfate
  4. filtrationAfter the resulting mixture was filtered
  5. concentrationthe filtrate was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-aa9ca4396b6e4bbb9113ced083fe7323
출처 데이터셋
uspto-grants-2003_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06627651B1

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