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Sodium sulfate decahydrate → (3-Benzyloxy-2-methyl-phenyl)-methanol

HRID 250638
ノート
印刷プレビュー

反応式

HRID 250638 の反応式
[CH2:1]([O:8][C:9]1[C:10]([CH3:18])=[C:11]([CH:15]=[CH:16][CH:17]=1)[C:12](O)=[O:13])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-].O.O.O.O.O.O.O.O.O.O.S([O-])([O-])(=O)=O.[Na+].[Na+]>O1CCCC1>[CH2:1]([O:8][C:9]1[C:10]([CH3:18])=[C:11]([CH2:12][OH:13])[CH:15]=[CH:16][CH:17]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 62649Sodium sulfate decahydrateHCID 118068023-Benzyloxy-2-methyl-benzoic acidHCID 21226445Aluminium lithium hydride

生成物 1

HCID 58087471(3-Benzyloxy-2-methyl-phenyl)-methanol

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of 3-benzyloxy-2-methyl-benzoic acid (621, 3.0 g, 0.012 mol) in tetrahydrofuran (100 mL), lithium aluminum hydride (25 mL, 1M solution in tetrahydrofuran, 0.025 mol) was added dropwise at 0° C. for 5 minutes. The reaction mixture was then stirred at room temperature overnight under an atmosphere of nitrogen. After sodium sulfate decahydrate (20.0 g, 0.062 mol) was added, the reaction mixture was stirred at room temperature for 10 minutes. A white solid was collected by filtration. The solid compound was further washed with a mixture of hexane and dichloromethane (9:1) and dried under high-vacuum (622, 2.8 g, 91%).

後処理

  1. stirringthe reaction mixture was stirred at room temperature for 10 minutes
  2. filtrationA white solid was collected by filtration
  3. washThe solid compound was further washed with a mixture of hexane and dichloromethane (9:1)
  4. customdried under high-vacuum (622, 2.8 g, 91%)

出典と根拠

ORDレコード
ord-d7faf417b3ac406495fe5c13c9f990ae
出典データセット
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07863288B2

反応ノート

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