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Sodium Methoxide → 4-Methoxy-7-phenyl-5,6,7,8-tetrahydroquinolin-5-one

HRID 1700507
ノート
印刷プレビュー

反応式

HRID 1700507 の反応式
Cl[C:2]1[C:11]2[C:10](=[O:12])[CH2:9][CH:8]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)[CH2:7][C:6]=2[N:5]=[CH:4][CH:3]=1.[CH3:19][O-:20].[Na+]>CO>[CH3:19][O:20][C:2]1[C:11]2[C:10](=[O:12])[CH2:9][CH:8]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)[CH2:7][C:6]=2[N:5]=[CH:4][CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 10942334Sodium MethoxideHCID 183173374-Chloro-7-phenyl-5,6,7,8-tetrahydroquinolin-5-one

生成物 1

HCID 183177154-Methoxy-7-phenyl-5,6,7,8-tetrahydroquinolin-5-one収率 92.9%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a solution of 4-chloro-7-phenyl-5,6,7,8-tetrahydroquinolin-5-one (0.23 g) in methanol (20 ml) was added sodium methoxide (0.096 g), and the mixture was refluxed for 1 hour and cooled. The solvent was evaporated, and to the residue was added ethyl acetate. The organic layer was washed with water and saturated brine, dried with magnesium sulfate and concentrated under reduced pressure, and the residue was recrystallized from ethyl acetate-hexane to give crystals of 4-methoxy-7-phenyl-5,6,7,8-tetrahydroquinolin-5-one (0.21 g).

後処理

  1. temperaturethe mixture was refluxed for 1 hour
  2. temperaturecooled
  3. customThe solvent was evaporated
  4. additionto the residue was added ethyl acetate
  5. washThe organic layer was washed with water and saturated brine
  6. dry with materialdried with magnesium sulfate
  7. concentrationconcentrated under reduced pressure
  8. customthe residue was recrystallized from ethyl acetate-hexane

出典と根拠

ORDレコード
ord-e735799c434340bfb4ecce0de73dd741
出典データセット
uspto-grants-2002_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06350749B1

反応ノート

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