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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 233285생성일: 2026년 10월 23일

Dimethylformamide → (E)-3-[2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]-5-pyridyl]acrylonitrile

https://huagongshe.com/ko/reaction/233285

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Lithium CarbonateHCID 11125—
반응물Lithium BromideHCID 82050—
반응물2-Bromo-3-[2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]-5-pyridyl]propionitrileHCID 10938527—
용매WaterHCID 962—
생성물(E)-3-[2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]-5-pyridyl]acrylonitrileHCID 2336135189%

반응 조건

온도120 °C

반응 단계

A mixture of 2-bromo-3-[2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]-5-pyridyl]propionitrile (4.5 g), lithium bromide (LiBr) (1.14 g), lithium carbonate (Li2CO3) (2.17 g) and N,N-dimethylformamide (50 ml) was stirred for 2.5 hours at 120° C. The reaction mixture was poured into water, which was subjected to extraction with ethyl acetate. The ethyl acetate layer was washed with water and dried (MgSO4), then the solvent was distilled off under reduced pressure to leave (E)-3-[2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]-5-pyridyl]acrylonitrile (3.2, 89%), which was recrystallized from ethyl acetate--hexane to give pale yellow crystals, m.p.116°-117° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05591862
출처 데이터셋uspto-grants-1997_01
ORD IDord-aa643455dbce476a92fbbdb8646e5997
출처 메모uspto-grants-1997_01