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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2221942생성일: 2026년 10월 27일

Dimethylformamide → ethyl (2E)-3-[5-({4-[(5-methyl-2-phenyl-1,3-oxazol-4-yl)methoxy]phenoxy}methyl)-2-phenyl-1,3-oxazol-4-yl]-2-propenoate

https://huagongshe.com/reaction/2221942

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Triethyl phosphonoacetateHCID 13345—
반응물Sodium hydrideHCID 24758—
반응물5-({4-[(5-Methyl-2-phenyl-1,3-oxazol-4-yl)methoxy]phenoxy}methyl)-2-phenyl-1,3-oxazole-4-carbaldehydeHCID 86605799—
용매WaterHCID 962—
생성물ethyl (2E)-3-[5-({4-[(5-methyl-2-phenyl-1,3-oxazol-4-yl)methoxy]phenoxy}methyl)-2-phenyl-1,3-oxazol-4-yl]-2-propenoateHCID 8660588749%

반응 단계

To a mixture of 5-({4-[(5-methyl-2-phenyl-1,3-oxazol-4-yl)methoxy]phenoxy}methyl)-2-phenyl-1,3-oxazole-4-carbaldehyde (1.0 g), ethyl diethylphosphonoacetate (0.52 g) and N,N-dimethylformamide (20 mL) was added sodium hydride (60% in oil, 0.10 g) at room temperature, and the mixture was stirred at the same temperature for 3 hrs. The reaction mixture was poured into water and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography to give ethyl (2E)-3-[5-({4-[(5-methyl-2-phenyl-1,3-oxazol-4-yl)methoxy]phenoxy}methyl)-2-phenyl-1,3-oxazol-4-yl]-2-propenoate as colorless crystals (0.55 g, yield 49%) from a fraction eluted with ethyl acetate-hexane (1:4, v/v). Recrystallization from ethyl acetate-hexane gave colorless prism crystals. melting point: 107-108° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07368578B2
출처 데이터셋uspto-grants-2008_05
ORD IDord-475c63da25ac4b1d818f97e8d10f90fe
출처 메모uspto-grants-2008_05