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Water → (2-(Aminomethyl)phenyl)methanol

HRID 2230802
ノート
印刷プレビュー

反応式

HRID 2230802 の反応式
[H-].[Al+3].[Li+].[H-].[H-].[H-].[C:7]([CH2:9][C:10]1C=C[CH:16]=[CH:15][C:11]=1C([O-])=O)#[N:8].O.[OH-].[Na+].C([O:24][CH2:25][CH3:26])C>>[OH:24][CH2:25][C:26]1[CH:16]=[CH:15][CH:11]=[CH:10][C:9]=1[CH2:7][NH2:8]
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 5

HCID 962Water2 回HCID 3283Diethyl EtherHCID 14798Sodium HydroxideHCID 69851902-(Cyanomethyl)benzoateHCID 21226445Aluminium lithium hydride

生成物 1

HCID 11275036(2-(Aminomethyl)phenyl)methanol

実験手順

Lithium aluminium hydride (12.4 ml, 1.0M in diethyl ether) was added cautiously to 2-cyanomethylbenzoate (1.00 g, 6.2 mmol) in anhydrous diethyl ether (40 ml) under nitrogen with stirring over 10 min. whilst ensuring the temperature was not greater than 15-25 C. using an ice bath. After the addition was complete the reaction mixture was allowed to warm to 21 C. and then heated at reflux for 16 h. The reaction mixture was cooled to approximately −10 C. It was treated cautiously dropwise with water (0.5 ml), 20% aqueous sodium hydroxide (0.37 ml) and water (1.74 ml). The resultant green heterogeous mixture was filtered and the residue was with diethyl ether (150 ml), the combined washings and filtrate were dried (MgSO4) and solvent was removed in vacuo affording the title compound as a green oil (0.807 g). Mass Spectrum m/z 138 (MH+ for C8H12NO).

後処理

  1. additionAfter the addition
  2. temperatureto warm to 21 C
  3. temperatureand then heated
  4. temperatureat reflux for 16 h
  5. temperatureThe reaction mixture was cooled to approximately −10 C
  6. filtrationThe resultant green heterogeous mixture was filtered
  7. dry with materialthe combined washings and filtrate were dried (MgSO4) and solvent
  8. customwas removed in vacuo

出典と根拠

ORDレコード
ord-490ca47ce448413182b239f7d2e8d01a
出典データセット
uspto-grants-2002_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06426337B1

反応ノート

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