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HRID 352072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/352072

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4-(Trifluoromethyl)cinnamamideHCID 5709014—
反応物Sodium Acetate TrihydrateHCID 23665404—
溶媒Dimethyl SulfoxideHCID 679—
溶媒MethanolHCID 887—
生成物4-(acetoxymethyl)-2-[(E)-2-[4-(trifluoromethyl)phenyl]ethenyl]-1,3-oxazoleHCID 1299284665%

反応条件

温度72.5 °C

反応手順

(E)-3-(4-(Trifluoromethyl)phenyl)-2-propenamide (10.0 g,46.5 mmol) and 1,3-dichloroacetone (11.0 g, 86.6 mmol) were added to toluene (50 ml), and the mixture was subjected to refluxing azeotropic dehydration using a Dean-Stark tube for 8.5 hours. The reaction mixture was concentrated under reduced pressure. To the residue were added dimethyl sulfoxide (50 ml) and sodium acetate trihydrate (15.8 g, 116.1 mmol). The mixture was stirred at 70-75° C. for 4 hours. Methanol (50 ml) was added. After allowing-to cool to room temperature and stirring; the mixture was stirred under ice-cooling for 1 hour. The precipitated crystals were collected by filtration, washed with cold-methanol (30 ml) and dried under reduced pressure to give 4-(acetoxymethyl)-2-[(E)-2-[4-(trifluoromethyl)phenyl]ethenyl]-1,3-oxazole (13.1 g, yield 65%).

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-6c7a09e552c3430f98ac75e781c5f0fa
出典メモuspto-grants-2004_06