ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

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

HRID 734482
ノート
印刷プレビュー

反応式

HRID 734482 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-de994c566245469aa291f3d09cf5d79b
出典データセット
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07592362B2

反応ノート

読み込み中…

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