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Acetic Anhydride → HCID 15007064, 화합물

HRID 1612655
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HRID 1612655 반응식
[CH3:1][C:2]1[CH:11]([CH3:12])[C:10](=[O:13])[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=1.[C:14](OC(=O)C)(=[O:16])[CH3:15]>>[C:14]([O:13][C:10]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=[C:2]([CH3:1])[C:11]=1[CH3:12])(=[O:16])[CH3:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 7918Acetic AnhydrideHCID 67692496HCID 67692496, 화합물

생성물 1

HCID 15007064HCID 15007064, 화합물

실험 절차

A solution of 1.73 g of 2,3-dimethyl-4-quinolone in 25 ml of acetic anhydride was stirred at 130° C. for 8 hours. The solution was evaporated to remove the solvent under reduced pressure, and 30 ml of chloroform was added to the solution. The mixture was washed with an aqueous saturated sodium hydrogen carbonate solution and water and dried over sodium sulfate. The solvent was evaporated under reduced pressure, and the crude product thus obtained was purified by silica gel column chromatography (Wako Gel C-200) to give 1.87 g of 4-acetoxy-2,3-dimethylquinoline.

후처리

  1. customThe solution was evaporated
  2. customto remove the solvent under reduced pressure, and 30 ml of chloroform
  3. additionwas added to the solution
  4. washThe mixture was washed with an aqueous saturated sodium hydrogen carbonate solution and water
  5. dry with material
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
dried over sodium sulfate
  • customThe solvent was evaporated under reduced pressure
  • customthe crude product thus obtained
  • customwas purified by silica gel column chromatography (Wako Gel C-200)
  • 출처 및 근거

    ORD 기록
    ord-51f6a0981d584821b05ed2840834126c
    출처 데이터셋
    uspto-grants-1993_03
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05190952

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