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Phosphorus oxychloride → 4-Chloro-6-methoxy-7-methyl-quinoline

HRID 228866
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HRID 228866 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][C:12]=1[CH3:13])[NH:9][CH:8]=[CH:7][C:6]2=O.P(Cl)(Cl)([Cl:17])=O>>[Cl:17][C:6]1[C:5]2[C:10](=[CH:11][C:12]([CH3:13])=[C:3]([O:2][CH3:1])[CH:4]=2)[N:9]=[CH:8][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 230784266-methoxy-7-methyl-1H-quinolin-4-one

생성물 1

HCID 230785384-Chloro-6-methoxy-7-methyl-quinoline수율 71%

실험 절차

6-Methoxy-7-methyl-1H-quinolin-4-one (73.9 g) was added to phosphorus oxychloride (160 ml), and the mixture was heated under reflux for 2 hr. The reaction solution was cooled to room temperature, and the solvent was then removed by distillation under the reduced pressure. Chloroform and water were added to the reaction solution, and the aqueous layer was neutralized with an aqueous potassium hydroxide solution. The organic layer was washed with water and saturated brine and was dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure, hexane was added to the residue, and the precipitated crystal was collected by filtration to give 4-chloro-6-methoxy-7-methyl-quinoline (12.7 g, yield 71%).

후처리

  1. temperature
the mixture was heated
  • temperatureunder reflux for 2 hr
  • customthe solvent was then removed by distillation under the reduced pressure
  • additionChloroform and water were added to the reaction solution
  • washThe organic layer was washed with water and saturated brine
  • dry with materialwas dried over anhydrous sodium sulfate
  • customThe solvent was removed by distillation under the reduced pressure, hexane
  • additionwas added to the residue
  • filtrationthe precipitated crystal was collected by filtration
  • 출처 및 근거

    ORD 기록
    ord-cc0010c1c67e428fa22bd8aa7247a880
    출처 데이터셋
    uspto-grants-2009_07
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07560558B2

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