反応 #927224

ord-c6d545108a58405c8cd8f7255340a5c8

反応方程式

COc1ccccc1
anisole
CC(=O)OC(C)=O
acetic anhydride
O=S(=O)([O-])[O-].[Mg+2]
magnesium sulfate
COc1ccc(C(C)=O)cc1
p-methoxyacetophenone
収率 97.2%

反応条件

温度
21°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    ろ過After filtration on Celite
  2. 2
    抽出the solution was extracted with three fractions of 50 ml ether
  3. 3
    洗浄the collected ether phase was washed with a saturated solution of potassium chloride
  4. 4
    乾燥After drying the ether phase

実験手順

The catalytic effect of the scandium salt of 5-trifluoromethanesulfonyl-1,3-dibutyl-2-sulfonyl-barbituric acid, obtained in Example 25, towards a Friedel-Crafts reaction of acylation was evaluated in the following manner. In 40 ml of anhydrous nitromethane, there is added 887 mg (0.7 moles) of the scandium salt of 5-trifluoromethylsulfonyl-1,3-dibutyl-2-sulfonyl-barbituric acid, and 1.08 g (10 mmoles) of anisole and 2.04 g (20 mmoles) of acetic anhydride. After stirring during 10 min at 21° C., the reaction mixture was diluted with 50 ml of ether and the reaction was inhibited with 100 ml of a saturated solution of sodium bicarbonate NaHCO3. After filtration on Celite, the solution was extracted with three fractions of 50 ml ether, then the collected ether phase was washed with a saturated solution of potassium chloride. After drying the ether phase with magnesium sulfate and evaporation, 1.46 g of p-methoxyacetophenone (95% yield) were recovered with a purity characterized by a proton RMN higher than 99%.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06365068B1uspto-grants-2002_04