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Methyl iodide → 3,8-Dimethoxy quinoline

HRID 399745
ノート
印刷プレビュー

反応式

HRID 399745 の反応式
[OH:1][C:2]1[CH:3]=[N:4][C:5]2[C:10]([CH:11]=1)=[CH:9][CH:8]=[CH:7][C:6]=2[O:12][CH3:13].[OH-].[K+].I[CH3:17]>C(O)C>[CH3:17][O:1][C:2]1[CH:3]=[N:4][C:5]2[C:10]([CH:11]=1)=[CH:9][CH:8]=[CH:7][C:6]=2[O:12][CH3:13]
参加物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 6328Methyl iodideHCID 14797Potassium HydroxideHCID 110843893-Quinolinol, 8-methoxy-2 回

生成物 1

HCID 105837983,8-Dimethoxy quinoline収率 87.3%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

175 mg of 3-hydroxy-8-methoxy quinoline [compound (V)] prepared in example 6 and 66 mg of potassium hydroxide were added to 3 ml of ethanol, and the solution was agitated for 30 minutes. To the solution was added 284 mg of iodomethane, and the solution was agitated for 24 hours. The solvent was removed, and the solution was extracted with dichloromethane. The dichloromethane layer was washed with water and aqueous sodium hydroxide, and dried with anhydrous magnesium sulfate. The dichloromethane was removed by vacuum distillation to give 165 mg of 3,8-dimethoxy quinoline.

後処理

  1. stirringthe solution was agitated for 24 hours
  2. customThe solvent was removed
  3. extractionthe solution was extracted with dichloromethane
  4. washThe dichloromethane layer was washed with water and aqueous sodium hydroxide
  5. dry with materialdried with anhydrous magnesium sulfate
  6. customThe dichloromethane was removed by vacuum distillation

出典と根拠

ORDレコード
ord-aaf958ebc6be4ebdac4f38df1b6371fc
出典データセット
uspto-grants-1998_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05824689

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート