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

HRID 242559

반응식

HRID 242559 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

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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-d139616e329d44ceabb8a5c420ff567d
출처 데이터셋
uspto-grants-2014_02
특허 번호
US08653096B2

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