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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2221835생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/2221835

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Tetraethyl methylenediphosphonateHCID 15455—
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—
생성물diethyl (E)-2-[5-({4-[(5-methyl-2-phenyl-1,3-oxazol-4-yl)methoxy]phenoxy}methyl)-2-phenyl-1,3-oxazol-4-yl]ethenylphosphonateHCID 8660579863.7%

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 (0.50 g), tetraethyl methylenediphosphonate (0.35 g) and N,N-dimethylformamide (10 mL) was added sodium hydride (60% in oil, 0.05 g) at room temperature, and the mixture was stirred at the same temperature for 1 hr. 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 diethyl (E)-2-[5-({4-[(5-methyl-2-phenyl-1,3-oxazol-4-yl)methoxy]phenoxy}methyl)-2-phenyl-1,3-oxazol-4-yl]ethenylphosphonate as colorless crystals (0.41 g, yield 62%) from a fraction eluted with ethyl acetate-hexane (2:1, v/v). Recrystallization from ethyl acetate-hexane gave colorless prism crystals. melting point: 124-125° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07368578B2
출처 데이터셋uspto-grants-2008_05
ORD IDord-5e5461717d704c81aa3f21d40fa99d86
출처 메모uspto-grants-2008_05