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1,3-Dimethyl-2-imidazolidinone → 4-Methoxy-2-methylquinolin-8-OL

HRID 864576
ノート
印刷プレビュー

反応式

HRID 864576 の反応式
Cl[C:2]1[C:11]2[C:6](=[C:7]([OH:12])[CH:8]=[CH:9][CH:10]=2)[N:5]=[C:4]([CH3:13])[CH:3]=1.CN1CCN(C)[C:16]1=[O:21].C[O-].[Na+]>CO>[OH:12][C:7]1[CH:8]=[CH:9][CH:10]=[C:11]2[C:6]=1[N:5]=[C:4]([CH3:13])[CH:3]=[C:2]2[O:21][CH3:16]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 66611,3-Dimethyl-2-imidazolidinoneHCID 10942334Sodium MethoxideHCID 122197224-Chloro-8-hydroxy-2-methylquinoline

生成物 1

HCID 183218914-Methoxy-2-methylquinolin-8-OL

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
150 °C

実験手順

A mixture of 4-chloro-8-hydroxy-2-methylquinoline (9 g), 1,3-dimethyl-2-imidazolidinone (100 ml) and 28% solution of sodium methoxide in methanol (135 ml) was stirred at 150° C. for 4 hours. The reaction mixture was cooled to ambient temperature followed by partition into ethyl acetate and water. The organic layer was washed with water and brine, dried over magnesium sulfate and concentrated in vacuo. The crystalline residue was washed with n-hexane to give 8-hydroxy-4-methoxy-2-methylquinoline (5.57 g).

後処理

  1. temperatureThe reaction mixture was cooled to ambient temperature
  2. customby partition into ethyl acetate and water
  3. washThe organic layer was washed with water and brine
  4. dry with materialdried over magnesium sulfate
  5. concentrationconcentrated in vacuo
  6. washThe crystalline residue was washed with n-hexane

出典と根拠

ORDレコード
ord-6cc47415f3164f418fca43b418f003ae
出典データセット
uspto-grants-1996_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05563162

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート