1-Phenyl-2-propen-1-one → 1,3-Dimethyl-3-(3-oxo-3-phenyl-propyl)-piperidin-4-one

HRID 576533

反応式

HRID 576533 の反応式
[CH3:1][N:2]1[CH2:7][CH2:6][C:5](=[O:8])[CH:4]([CH3:9])[CH2:3]1.O1CCOCC1.[OH-].[K+].[C:18]1([C:24](=[O:27])[CH:25]=[CH2:26])[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>O>[CH3:1][N:2]1[CH2:7][CH2:6][C:5](=[O:8])[C:4]([CH3:9])([CH2:26][CH2:25][C:24](=[O:27])[C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[CH2:3]1

参加物

6

反応条件

温度
25 °C

実験手順

To a stirred solution of 1,3-dimethyl-piperidin-4-one (0.1 g, 0.787 mmol) in mixture of 1,4 dioxane (2 mL) and water (0.1 mL) was added crushed KOH (44 mg, 0.787 mmol). The reaction mixture was stirred at 25° C. for 10 min. To this was added 1-phenylprop-2-en-1-one (103 mg, 0.787 mmol) dropwise. The reaction mixture was stirred at 25° C. for 2 h. The reaction mixture was concentrated under reduced pressure and the residue was diluted with water (10 mL) and EtOAc (20 mL), the organic layer was separated, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The resulting crude product was purified by column chromatography on neutral alumina (eluted with EtOAc:Hexanes, 1:99) to afford 1,3-dimethyl-3-(3-oxo-3-phenyl-propyl)-piperidin-4-one as an oil (22 mg).

後処理

  1. additionwas added
  2. stirringThe reaction mixture was stirred at 25° C. for 2 h
  3. concentrationThe reaction mixture was concentrated under reduced pressure
  4. additionthe residue was diluted with water (10 mL) and EtOAc (20 mL)
  5. customthe organic layer was separated
  6. dry with materialdried over anhydrous sodium sulfate
  7. concentrationconcentrated under reduced pressure
  8. customThe resulting crude product was purified by column chromatography on neutral alumina (eluted with EtOAc:Hexanes, 1:99)

出典と根拠

ORDレコード
ord-0c551d20fef6440ca1f200327530665c
出典データセット
uspto-grants-2015_05
特許番号
US09040519B2

関連ノート

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