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Aluminium lithium hydride → (3S)-3-(Propan-2-yl)morpholine

HRID 249847
ノート
印刷プレビュー

反応式

HRID 249847 の反応式
[H-].[Al+3].[Li+].[H-].[H-].[H-].[CH:7]([C@@H:10]1[NH:15][C:14](=O)[CH2:13][O:12][CH2:11]1)([CH3:9])[CH3:8]>C1COCC1>[CH:7]([C@H:10]1[CH2:11][O:12][CH2:13][CH2:14][NH:15]1)([CH3:9])[CH3:8]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 21226445Aluminium lithium hydrideHCID 55288043HCID 55288043、化合物

生成物 1

HCID 53338727(3S)-3-(Propan-2-yl)morpholine収率 83%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To ice-cold THF (6 mL) was added lithium aluminum hydride (1.0 M solution in THF, 18.0 mL, 18.0 mmol). Once the addition was complete, a solution of (S)-5-isopropylmorpholin-3-one (1.3 g, 9.0 mmol) in THF (6 mL) was added dropwise over 20 min. Once the addition was completed, the ice bath was removed and the reaction mixture stirred at reflux for 18 h. The reaction was cooled in an ice-bath and to this was slowly added H2O (0.75 mL), then a 15% aqueous solution of NaOH (0.75 mL), and then H2O (0.75 mL). The resulting mixture was stirred at room temperature for 1 h and then filtered washing the solid with EtOAc (50 mL). The filtrate was concentrated at room temperature under reduced pressure to provide (S)-3-isopropylmorpholine (0.96 g, 83%) as a clear, colorless oil. 1H NMR and MS consistent.

後処理

  1. additionOnce the addition
  2. additionOnce the addition
  3. customthe ice bath was removed
  4. temperatureat reflux for 18 h
  5. temperatureThe reaction was cooled in an ice-bath
  6. stirringThe resulting mixture was stirred at room temperature for 1 h
  7. filtrationfiltered
  8. washwashing the solid with EtOAc (50 mL)
  9. concentrationThe filtrate was concentrated at room temperature under reduced pressure

出典と根拠

ORDレコード
ord-d1f917648eb147ca8512badbe86381d5
出典データセット
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07863271B2

反応ノート

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