Sodium hydride → 4-Cyclopropylmethoxyindole

HRID 1003540노트

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HRID 1003540 반응식
[OH:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]=[CH:5][NH:6]2.[H-].[Na+].[CH:13]1([CH2:16]Br)[CH2:15][CH2:14]1>CN(C)C=O>[CH:13]1([CH2:16][O:1][C:2]2[CH:10]=[CH:9][CH:8]=[C:7]3[C:3]=2[CH:4]=[CH:5][NH:6]3)[CH2:15][CH2:14]1

참가 물질

5

실험 절차

A solution of 5.00 gm (37.6 mMol) 4-hydroxyindole in dimethylformamide was added dropwise over 30 minutes to a solution of 1.65 gm (41.3 mMol) sodium hydride (60% suspension in mineral oil) in 25 mL dimethylformamide at 0° C. The resulting black solution was stirred at room temperature for 2 hours and then a solution of 3.6 mL (37.6 mMol) cyclopropylmethyl bromide in 10 mL dimethylformamide was added dropwise. The resulting mixture was stirred for 1.5 hours at room temperature. The reaction mixture was then quenched by the addition of 100 mL water and the resulting mixture extracted well with ethyl acetate. The organic phases were combined, washed sequentially with water and saturated aqueous sodium chloride, dried over sodium sulfate and concentrated under reduced pressure. The residue was subjected to silica gel chromatography, eluting with 10% ethyl acetate in hexane. Fractions shown to contain product were combined and concentrated under reduced pressure to provide 4.48 gm (64%) of the title compound as an amber oil.

후처리

  1. stirringThe resulting mixture was stirred for 1.5 hours at room temperature
  2. customThe reaction mixture was then quenched by the addition of 100 mL water
  3. extractionthe resulting mixture extracted well with ethyl acetate
  4. washwashed sequentially with water and saturated aqueous sodium chloride
  5. dry with materialdried over sodium sulfate
  6. concentrationconcentrated under reduced pressure
  7. washeluting with 10% ethyl acetate in hexane
  8. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-9b49c834906c48998b378515f5c47c78
출처 데이터셋
uspto-grants-2000_04
특허 번호
US06046215

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