Methyl iodide → 1-Benzyl-3,5-dimethylpiperidin-4-one

HRID 457074

反応式

HRID 457074 の反応式
[CH2:1]([N:8]1[CH2:13][CH2:12][C:11](=[O:14])[CH:10]([CH3:15])[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH:16]([N-]C(C)C)(C)C.[Li+].IC>C1COCC1>[CH2:1]([N:8]1[CH2:13][CH:12]([CH3:16])[C:11](=[O:14])[CH:10]([CH3:15])[CH2:9]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

参加物

5

反応条件

温度
-78 °C

実験手順

To 1-benzyl-3-methyl-4-piperidone (2.0 g, 9.8 mmol) in THF at about −78° C. under argon, was added Lithium diisopropylamide (7.35 mL, 14.7 mmol, 2 M in heptane/THF/ethylbenzene). After stirring for about 1 hour at about −78° C., iodomethane (0.73 mL, 11.8 mmol) was added. The reaction mixture was stirred for about 1 hour at about −78° C., then warmed to room temperature. Stirring was continued overnight at room temperature. The reaction was quenched with saturated ammonium chloride solution, and extracted with ethyl acetate. The organic layer was washed with water, then brine and dried over magnesium sulfate. The crude product was chromatographed on silica gel, eluting with EtOAc/hexane (3:10) to give a yellow oil of the title compound.

後処理

  1. stirringThe reaction mixture was stirred for about 1 hour at about −78° C.
  2. temperaturewarmed to room temperature
  3. stirringStirring
  4. waitwas continued overnight at room temperature
  5. customThe reaction was quenched with saturated ammonium chloride solution
  6. extractionextracted with ethyl acetate
  7. washThe organic layer was washed with water
  8. dry with materialbrine and dried over magnesium sulfate
  9. customThe crude product was chromatographed on silica gel
  10. washeluting with EtOAc/hexane (3:10)

出典と根拠

ORDレコード
ord-b91370b5b662404cbe1635393214a6f0
出典データセット
uspto-grants-2007_03
特許番号
US07186729B2

関連ノート

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