Dimethyl Sulfate → 2,2-Dimethoxy-1-methylpyrrolidine

HRID 60403

반응식

HRID 60403 반응식
[CH3:1][N:2]1[CH2:6][CH2:5][CH2:4][C:3]1=[O:7].S(OC)([O:11][CH3:12])(=O)=O.[CH3:15][O-].[Na+]>CO>[CH3:15][O:7][C:3]1([O:11][CH3:12])[CH2:4][CH2:5][CH2:6][N:2]1[CH3:1]

참가 물질

5

반응 조건

온도
90 °C

실험 절차

To a mixture containing 10 mL (10.28 g, 104 mmol) of N-methyl-2-pyrrolidinone and 10 mL (13.25 g, 105 mmol) of dimethyl sulfate was stirred and heated at 90° C. for 1.5 h, then allowed to cool to room temperature. A solution containing 25 mL of 25% methanolic sodium methoxide and 72 mL of methanol was added at −10° C. under Ar over a period of 1 h. The precipitated solid was filtered and the solvent was concentrated under diminished pressure. The residue was dissolved in 100 mL of ether and stirred for 1 h, then the precipitated solid was filtered. The solid was washed with two 10-mL portions of ether. After concentration under diminished pressure, the residue was distilled in vacuo to give 2,2-dimethoxy-1-methylpyrrolidine as a yellow liquid: yield 4.42 g (29%); 1H NMR (CDCl3) δ 1.62-1.74 (m, 2H), 1.83 (t, 2H, J=7.8 Hz), 2.28 (s, 3H), 2.78 (t, 2H, J=6.6 Hz), 3.15 (s, 3H).

후처리

  1. temperatureto cool to room temperature
  2. additionwas added at −10° C. under Ar over a period of 1 h
  3. filtrationThe precipitated solid was filtered
  4. concentrationthe solvent was concentrated under diminished pressure
  5. dissolutionThe residue was dissolved in 100 mL of ether
  6. stirringstirred for 1 h
  7. filtrationthe precipitated solid was filtered
  8. washThe solid was washed with two 10-mL portions of ether
  9. concentrationAfter concentration under diminished pressure
  10. distillationthe residue was distilled in vacuo

출처 및 근거

ORD 기록
ord-0ab3344e38254bd8b1a434f63f4d62d8
출처 데이터셋
uspto-grants-2016_09
특허 번호
US09440967B2

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