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HRID 352073作成日:2026年10月26日

Toluene → 4-(acetoxymethyl)-2-[(E)-2-[4-(trifluoromethyl)phenyl]ethenyl]-1,3-oxazole

https://huagongshe.com/reaction/352073

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物1,3-DichloroacetoneHCID 10793—
反応物Sodium AcetateHCID 517045—
反応物4-(Trifluoromethyl)cinnamamideHCID 5709014—
溶媒Dimethyl SulfoxideHCID 679—
溶媒MethanolHCID 887—
生成物4-(acetoxymethyl)-2-[(E)-2-[4-(trifluoromethyl)phenyl]ethenyl]-1,3-oxazoleHCID 1299284651%

反応条件

温度75 °C

反応手順

(E)-3-(4-(Trifluoromethyl)phenyl)-2-propenamide (950 g, 4.42 mol) and 1,3-dichloroacetone (1045 g, 8.23 mol)were added to toluene (4.75 L) and the mixture was subjected to refluxing azeotropic dehydration using a Dean-Stark tube for 8 hours. During the reaction, an azeotropic mixture (2.38 L) was removed. The reaction mixture was concentrated under reduced pressure, and dimethyl sulfoxide (4.75L) and sodium acetate (905 g, 11.0 mol) were added to the residue. The mixture was stirred at 70-80° C. for 3.5 hours. Methanol (4.75 L) was added. After allowing to cool to room temperature and stirring, the mixture was stirred for 1 hour under ice-cooling. The precipitated crystals were collected by filtration, washed with cold-methanol (1.9 L), and dried under reduced pressure to give 4-(acetoxymethyl)-2-[(E)-2-[4-(trifluoromethyl)phenyl]ethenyl]-1,3-oxazole (1560 g, yield 51%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06743924B2
出典データセットuspto-grants-2004_06
ORD IDord-87acf2d9cbc24512b9fdde5a0a549b33
出典メモuspto-grants-2004_06