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

HRID 228866
ノート
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反応式

HRID 228866 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

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

生成物 1

HCID 230785384-Chloro-6-methoxy-7-methyl-quinoline収率 71%

実験手順

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%).

後処理

  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
  • 出典と根拠

    ORDレコード
    ord-cc0010c1c67e428fa22bd8aa7247a880
    出典データセット
    uspto-grants-2009_07
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US07560558B2

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