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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 352073생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/352073

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물1,3-DichloroacetoneHCID 10793—
반응물Sodium AcetateHCID 517045—
반응물4-(Trifluoromethyl)cinnamamideHCID 5709014—
용매Dimethyl SulfoxideHCID 679—
용매MethanolHCID 887—
생성물4-(acetoxymethyl)-2-[(E)-2-[4-(trifluoromethyl)phenyl]ethenyl]-1,3-oxazoleHCID 1299284651%

반응 조건

온도75 °C

반응 단계

(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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06743924B2
출처 데이터셋uspto-grants-2004_06
ORD IDord-87acf2d9cbc24512b9fdde5a0a549b33
출처 메모uspto-grants-2004_06