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

HRID 1169488
ノート
印刷プレビュー

反応式

HRID 1169488 の反応式
[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]
参加物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 14798Sodium HydroxideHCID 21226445Aluminium lithium hydrideHCID 70025127Ethyl 2-propoxycinnamate

生成物 1

HCID 229900333-(2-Propoxyphenyl)-1-propanol収率 96.8%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒3 回

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-aa9ca4396b6e4bbb9113ced083fe7323
出典データセット
uspto-grants-2003_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06627651B1

反応ノート

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