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(5S)-5-Phenyl-3-morpholinone → (S)-3-phenylmorpholine

HRID 595973
ノート
印刷プレビュー

反応式

HRID 595973 の反応式
[H-].[H-].[H-].[H-].[Li+].[Al+3].C1COCC1.[C:12]1([C@@H:18]2[NH:23][C:22](=O)[CH2:21][O:20][CH2:19]2)[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>C1COCC1>[C:12]1([C@H:18]2[CH2:19][O:20][CH2:21][CH2:22][NH:23]2)[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1
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 11105904(5S)-5-Phenyl-3-morpholinoneHCID 68718528lithium aluminium hydride THF

生成物 1

HCID 22860773(S)-3-phenylmorpholine収率 96%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a LiAlH4/THF slurry (0.47 g/2 mL) was added dropwise (S)-5-phenylmorpholin-3-one in THF solution (481 mg in 6 mL) at room temperature over 5 min. The resulting mixture was stirred at room temperature thereafter for 1 hour, then was heated with 72° C. oil bath overnight, then was cooled down to 0° C., quenched by sequential addition of H2O (0.47 mL), 3M aqueous solutionueous NaOH (0.47 mL) and H2O (1.4 mL), and the quenched residue was diluted with Et2O (30 mL), stirred for 10 min and the ethereal solution was separated by filtration. The filtrate was concentrated, further dried under vacuum and (S)-3-phenylmorpholine (424 mg, 96% yield) was obtained as colorless solid. LCMS (m/z): 164.2 (MH+), 0.33 min.

後処理

  1. temperaturewas heated with 72° C. oil bath overnight
  2. temperaturewas cooled down to 0° C.
  3. customquenched by sequential addition of H2O (0.47 mL), 3M aqueous solutionueous NaOH (0.47 mL) and H2O (1.4 mL)
  4. additionthe quenched residue was diluted with Et2O (30 mL)
  5. stirringstirred for 10 min
  6. customthe ethereal solution was separated by filtration
  7. concentrationThe filtrate was concentrated
  8. customfurther dried under vacuum

出典と根拠

ORDレコード
ord-4d9fb5b0a78e48f7b6dcbaa8e988c92f
出典データセット
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09242996B2

反応ノート

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