戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 602237作成日:2026年10月26日

Anisole → 4'-Methoxyacetophenone

https://huagongshe.com/reaction/602237

反応式

関与物質

役割名称HCID仕込み量
反応物AnisoleHCID 7519—
反応物Acetic AnhydrideHCID 7918—
反応物Sulfuric acid magnesium salt (1:1)HCID 24083—
反応物3-Trifluoromethyl-5-trifluoromethanesulfonyl-1,2,4-triazoleHCID 178527382—
触媒ScandiumHCID 23952—
溶媒Diethyl EtherHCID 3283—
溶媒NitromethaneHCID 6375—
生成物4'-MethoxyacetophenoneHCID 747697.2%

反応条件

温度21 °C

反応手順

The catalytic effect of the scandium salt of 3-trifluoromethyl-5-trifluoromethanesulfonyl-1,2,4-triazole, obtained in Example 3, relative to a reaction was evaluated in the following manner. In 40 ml of anhydrous nitromethane, there is added 592 mg (700 .mu.moles) of the scandium salt of 3-trifluoromethyl-5-trifluoromethanesulfonyl-1,2,-4-triazole, and 1.08 g (10 mmoles) of anisol and 2.04 g 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 by 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, and 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 (97% yield) was collected, with a purity characterized by a proton NMR higher than 99%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07906235B2
出典データセットuspto-grants-2011_03
ORD IDord-0f4f1a9a186a4902a9a8aeae64d7416f
出典メモuspto-grants-2011_03