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Acetic Anhydride → HCID 15007064、化合物

HRID 1612655
ノート
印刷プレビュー

反応式

HRID 1612655 の反応式
[CH3:1][C:2]1[CH:11]([CH3:12])[C:10](=[O:13])[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=1.[C:14](OC(=O)C)(=[O:16])[CH3:15]>>[C:14]([O:13][C:10]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=[C:2]([CH3:1])[C:11]=1[CH3:12])(=[O:16])[CH3:15]
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 7918Acetic AnhydrideHCID 67692496HCID 67692496、化合物

生成物 1

HCID 15007064HCID 15007064、化合物

実験手順

A solution of 1.73 g of 2,3-dimethyl-4-quinolone in 25 ml of acetic anhydride was stirred at 130° C. for 8 hours. The solution was evaporated to remove the solvent under reduced pressure, and 30 ml of chloroform was added to the solution. The mixture was washed with an aqueous saturated sodium hydrogen carbonate solution and water and dried over sodium sulfate. The solvent was evaporated under reduced pressure, and the crude product thus obtained was purified by silica gel column chromatography (Wako Gel C-200) to give 1.87 g of 4-acetoxy-2,3-dimethylquinoline.

後処理

  1. customThe solution was evaporated
  2. customto remove the solvent under reduced pressure, and 30 ml of chloroform
  3. additionwas added to the solution
  4. washThe mixture was washed with an aqueous saturated sodium hydrogen carbonate solution and water
  5. dry with material
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
dried over sodium sulfate
  • customThe solvent was evaporated under reduced pressure
  • customthe crude product thus obtained
  • customwas purified by silica gel column chromatography (Wako Gel C-200)
  • 出典と根拠

    ORDレコード
    ord-51f6a0981d584821b05ed2840834126c
    出典データセット
    uspto-grants-1993_03
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US05190952

    反応ノート

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