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Ethanol → 5-Chloro-2-methylsulfonylindan-1-one

HRID 1884083
ノート
印刷プレビュー

反応式

HRID 1884083 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[C:7](=[O:11])[CH:6](SC)[CH2:5]2.[S:14]([O:18]OS([O-])(=O)=O)(O)(=O)=[O:15].[K+].[CH2:25](O)C>O>[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[C:7](=[O:11])[CH:6]([S:14]([CH3:25])(=[O:18])=[O:15])[CH2:5]2
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 702EthanolHCID 99207715-Chloro-2-methylsulfanylindan-1-oneHCID 23690007Potassium hydrogen persulfate

生成物 1

HCID 99648205-Chloro-2-methylsulfonylindan-1-one

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

0.5 g of 5-chloro-2-methylsulfanylindan-1-one was dissolved in 10 ml of dry ethanol. At 0° C., a solution of 4.33 g of potassium hydrogenpersulfate (2 KHSO5×KHSO4×K2SO4; “Oxone”) in 10 ml of water was added dropwise and the reaction mixture was then stirred at room temperature for 5 h. The alcohol was distilled off under reduced pressure at room temperature. 20 ml of dichloromethane and 10 ml of water was added to the residue, and the mixture was stirred for 10 min. The organic phase was separated off, dried over magnesium sulfate, filtered and concentrated under reduced pressure, and the residue was dried. This gave 5-chloro-2-methylsulfonylindan-1-one of melting point 196° C.

後処理

  1. distillationThe alcohol was distilled off under reduced pressure at room temperature
  2. addition20 ml of dichloromethane and 10 ml of water was added to the residue
  3. stirringthe mixture was stirred for 10 min
  4. customThe organic phase was separated off
  5. dry with materialdried over magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure
  8. customthe residue was dried

出典と根拠

ORDレコード
ord-f713b5f61dc2411fb717b0053249ec4d
出典データセット
uspto-grants-2004_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06762326B2

反応ノート

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