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Water → N-Methylindan-2-amine

HRID 1531283
ノート
印刷プレビュー

反応式

HRID 1531283 の反応式
C(O[C:4]([NH:6][CH:7]1[CH2:15][C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[CH2:8]1)=O)C.C(=O)(O)N.[H-].[H-].[H-].[H-].[Li+].[Al+3].O.[OH-].[Na+]>CCOCC>[CH3:4][NH:6][CH:7]1[CH2:15][C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[CH2:8]1
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 21253362Carbamate 2-(ethoxycarbonyl-amino)indane

生成物 1

HCID 15023225N-Methylindan-2-amine

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒2 回

実験手順

Under a nitrogen atmosphere, a solution of the carbamate 2-(ethoxycarbonyl-amino)indane (6.07 g, 29.6 mmol) in Et2O (100 mL) is added slowly to a mixture of LiAlH4 (1.70 g, 44.7 mmol) in Et2O (100 ml) chilled at 0°. The resulting mixture is stirred for 18 h and allowed to warm to 20°. The reaction mixture is re-chilled to 0° and treated cautiously with H2O (1.7 mL), 15% NaOH (1.7 mL) and again H2O (5.1 mL). The mixture is stirred for 20 minutes, warming slowly to 20°. The precipitate is vacuum filtered and the filtrate extracted into 1N HCl. The acid solution is washed with fresh Et2O, then basified with cold 1N NaOH. The cloudy mixture is extracted with Et2O, washed with saturated brine, dried over Na2SO4, is filtered and concentrated to an oil.

後処理

  1. temperaturechilled at 0°
  2. temperatureto warm to 20°
  3. temperatureThe reaction mixture is re-chilled to 0°
  4. stirringThe mixture is stirred for 20 minutes
  5. temperaturewarming slowly to 20°
  6. filtrationfiltered
  7. extractionthe filtrate extracted into 1N HCl
  8. washThe acid solution is washed with fresh Et2O
  9. extractionThe cloudy mixture is extracted with Et2O
  10. washwashed with saturated brine
  11. dry with materialdried over Na2SO4
  12. filtrationis filtered
  13. concentrationconcentrated to an oil

出典と根拠

ORDレコード
ord-e81d0e3be9934d94842c5994466059d5
出典データセット
uspto-grants-2001_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06197798B1

反応ノート

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