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p-Toluenesulfonic acid → Ethyl (2-bromo-4,5-difluorobenzoyl)acetate

HRID 1788658
ノート
印刷プレビュー

反応式

HRID 1788658 の反応式
[Br:1][C:2]1[CH:20]=[C:19]([F:21])[C:18]([F:22])=[CH:17][C:3]=1[C:4]([CH:6](C(OCC)=O)[C:7]([O:9][CH2:10][CH3:11])=[O:8])=[O:5].C1(C)C=CC(S(O)(=O)=O)=CC=1>O>[Br:1][C:2]1[CH:20]=[C:19]([F:21])[C:18]([F:22])=[CH:17][C:3]=1[C:4]([CH2:6][C:7]([O:9][CH2:10][CH3:11])=[O:8])=[O:5]
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 6101p-Toluenesulfonic acidHCID 14347789Diethyl (2-bromo-4,5-difluorobenzoyl)malonate

生成物 1

HCID 13912599Ethyl (2-bromo-4,5-difluorobenzoyl)acetate収率 84.9%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

To a solution of diethyl (2-bromo-4,5-difluorobenzoyl)malonate (75.6 g) in water (100 ml) is added p-toluenesulfonic acid (0.3 g), and the mixture is refluxed for 3 hours. After cooling, the reaction mixture is extracted with dichloromethane. The dichloromethane layer is washed with saturated aqueous sodium chloride solution and dried over magnesium sulfate. After distilling off the solvent under reduced pressure, the residue is distilled to give ethyl (2-bromo-4,5-difluorobenzoyl)acetate (52.0 g), b.p. 105°-115° C. (0.15 mmHg).

後処理

  1. temperaturethe mixture is refluxed for 3 hours
  2. temperatureAfter cooling
  3. extractionthe reaction mixture is extracted with dichloromethane
  4. washThe dichloromethane layer is washed with saturated aqueous sodium chloride solution
  5. dry with materialdried over magnesium sulfate
  6. distillationAfter distilling off the solvent under reduced pressure
  7. distillationthe residue is distilled

出典と根拠

ORDレコード
ord-b28196377e324dcfbda86271a54c7717
出典データセット
uspto-grants-1987_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04684648

反応ノート

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