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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 352079생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/352079

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물1,3-DichloroacetoneHCID 10793—
반응물Potassium CarbonateHCID 11430—
반응물4-(Trifluoromethyl)cinnamamideHCID 5709014—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물4-(hydroxymethyl)-2-[(E)-2-[4-(trifluoromethyl)phenyl]ethenyl]-1,3-oxazoleHCID 1299284762%

반응 단계

(E)-3-(4-(Trifluoromethyl)phenyl)-2-propenamide (4.30 g, 20.0 mmol) and 1,3-dichloroacetone (4.75 g, 37.4 mmol) were added to toluene (20 ml) and the mixture was subjected to refluxing azeotropic dehydration using a Dean-Stark tube for 6 hours. The reaction mixture was allowed to cool to room temperature, and DMF (50 ml), water (30 ml) and potassium carbonate (13.7 g, 99.1 mmol) were added. The mixture was stirred at 100° C. for 1.5 hours. After allowing to cool to room temperature, ethyl acetate (200 ml) and water (150 ml) were added and the mixture was partitioned. The organic layer was washed with water/saturated brine (1:1, 100 ml). To the organic layer was added ethyl acetate (400 ml), and the mixture was washed with water (200 ml) twice and concentrated under reduced pressure. Ethanol (30 ml) was added to the residue. Water (38 ml) was added and the precipitated crystals were collected by filtration, washed with water (40 ml) and dried under reduced pressure to give 4-(hydroxymethyl)-2-[(E)-2-[4-(trifluoromethyl)phenyl]ethenyl]-1,3-oxazole (3.3 g, 3.71 mmol, yield 62%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06743924B2
출처 데이터셋uspto-grants-2004_06
ORD IDord-0a8d5c38ed564c68853174856e713334
출처 메모uspto-grants-2004_06