反応 #1160

ord-b9e829672ee641d4912a1f2c034f3d35

反応方程式

[Al+3].[Cl-].[Cl-].[Cl-]
AlCl3
CSc1ccccc1
thioanisole
CC(=O)Cl
acetyl chloride
CSc1ccc(C(C)=O)cc1
4-(methylthio)acetophenone
収率 88.1%

溶媒

反応条件

温度
0°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.ADDITIONaddition
  2. 2
    その他does not exceed 10° C
  3. 3
    温度heated for 1 h at 40° C.
  4. 4
    その他The resulting mixture is separated
  5. 5
    抽出extracted with CH2Cl2
  6. 6
    洗浄washed with water
  7. 7
    乾燥dried over MgSO4
  8. 8
    濃縮concentrated

実験手順

123 g (0.92 mol) of AlCl3 are added with a spatula to a mixture of 100 g (0.8 mol) of thioanisole, 750 ml of CH2Cl2 and 63 ml (0.9 mol) of acetyl chloride, cooled to 0° C. beforehand, said addition being carried out so that the temperature does not exceed 10° C. The mixture is stirred for 1 h at room temperature, heated for 1 h at 40° C. and then poured into 800 ml of an ice/water mixture. The resulting mixture is separated and extracted with CH2Cl2. The organic phases are combined, washed with water and then dried over MgSO4 and concentrated to give 117.1 g of 4-(methylthio)acetophenone.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05723485uspto-grants-1998_03