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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2120316생성일: 2026년 10월 27일

Hydrochloric Acid → 3-(4-nitrophenyl)prop-2-enoyl Chloride

https://huagongshe.com/reaction/2120316

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Ethyl AcetateHCID 8857—
반응물Thionyl ChlorideHCID 24386—
반응물2-Propenoic acid, 3-(4-nitrophenyl)-HCID 70156—
용매DimethylformamideHCID 6228—
생성물3-(4-nitrophenyl)prop-2-enoyl ChlorideHCID 31946399.2%

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 번호US06689899B2
출처 데이터셋uspto-grants-2004_02
ORD IDord-fdb31367611f40619b8ef82bc1701b31
출처 메모uspto-grants-2004_02