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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 380721생성일: 2026년 10월 23일

4-Nitrophenol → (4'-Nitrophenyl)-4-nitrocinnamate

https://huagongshe.com/ko/reaction/380721

반응식

참여 물질

역할이름HCID투입량
반응물4-NitrophenolHCID 980—
반응물PyridineHCID 1049—
반응물3-(4-nitrophenyl)prop-2-enoyl ChlorideHCID 319463—
용매AcetoneHCID 180—
생성물(4'-Nitrophenyl)-4-nitrocinnamateHCID 5371111395.5%

반응 조건

온도50 °C

반응 단계

193.2 g (1 mole) of 4-nitrocinnamic acid and 650 g of ethyl acetate were placed in a reaction vessel. While 200 g of thionyl chloride with some drops of DMF was dropped into the reaction mixtures, the reaction mixtures were refluxed with stirring until the generation of hydrogen chloride gas stopped. The reacted solution was concentrated until a solid could be precipitated and was poured into hexane and then the precipitated solid was separated by filtration and dried. 210 g of 4-nitrocinnamoyl chloride was yielded. 64.5 g (0.3 mole) of 4-nitrocinnamoyl chloride and 300 g of acetone were placed in a reaction vessel. The reaction mixtures were heated at 50° C. with stirring under a nitrogen current. 41.73 g (0.3 mole) of 4-nitrophenol, 60 g of pyridine, and 300 g of acetone were added dropwise to the above reaction vessel using a dropping funnel. After the completion of the addition, the reaction mixtures were refluxed with stirring under a nitrogen current for 2 hours. After the reaction, a precipitate was separated by filtration, and the filtrated solid was washed by water and dried. 90 g of light yellow colored needle-like crystals ((4-nitrophenyl)-4-cinnamate)was yielded.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06303742B1
출처 데이터셋uspto-grants-2001_10
ORD IDord-086338c2e6a64c31862edfe61a8af3d1
출처 메모uspto-grants-2001_10