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Water → 1-(2-Bromo-3,5,6-trimethylphenyl)ethanone

HRID 1985907
ノート
印刷プレビュー

反応式

HRID 1985907 の反応式
[Br:1][C:2]1[CH:7]=[C:6]([CH3:8])[C:5]([CH3:9])=[CH:4][C:3]=1[CH3:10].[C:11](Cl)(=[O:13])[CH3:12].[Cl-].[Al+3].[Cl-].[Cl-].O>ClCCl>[Br:1][C:2]1[C:3]([CH3:10])=[CH:4][C:5]([CH3:9])=[C:6]([CH3:8])[C:7]=1[C:11](=[O:13])[CH3:12]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 6367Acetyl chlorideHCID 796101-Bromo-2,4,5-trimethylbenzeneHCID 6451240Aluminum(III) Chloride

生成物 1

HCID 866136691-(2-Bromo-3,5,6-trimethylphenyl)ethanone収率 91.2%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

To a mixture of 1-bromo-2,4,5-trimethylbenzene (5.0 g, 25.0 mmol) and acetyl chloride (2.45 ml, 34.5 mmol) in dichloromethane (50 ml) was added aluminium chloride (4.42 g, 33.1 mmol) in dichloromethane (50 ml) and the reaction mixture was stirred at room temperature for 18 h. The mixture was poured into water and the two layers were separated. The organic phase was washed with saturated aqueous sodium hydrogen carbonate solution, dried (MgSO4) and filtered through silica. The filtrate was concentrated in vacuo to give the title compound (5.50 g).

後処理

  1. customthe two layers were separated
  2. washThe organic phase was washed with saturated aqueous sodium hydrogen carbonate solution
  3. dry with materialdried (MgSO4)
  4. filtrationfiltered through silica
  5. concentrationThe filtrate was concentrated in vacuo

出典と根拠

ORDレコード
ord-df4779b1902f4751b652d7b877f1d292
出典データセット
uspto-grants-2009_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07547718B2

反応ノート

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