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

HRID 457074

반응식

HRID 457074 반응식
[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

참가 물질

5

반응 조건

온도
-78 °C

실험 절차

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.

후처리

  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)

출처 및 근거

ORD 기록
ord-b91370b5b662404cbe1635393214a6f0
출처 데이터셋
uspto-grants-2007_03
특허 번호
US07186729B2

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