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HRID 380721作成日:2026年10月25日

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

https://huagongshe.com/reaction/380721

反応式

関与物質

役割名称HCID仕込み量
反応物4-NitrophenolHCID 980—
反応物PyridineHCID 1049—
反応物3-(4-nitrophenyl)prop-2-enoyl ChlorideHCID 319463—
溶媒AcetoneHCID 180—
生成物(4'-Nitrophenyl)-4-nitrocinnamateHCID 5371111395.5%

反応条件

温度50 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06303742B1
出典データセットuspto-grants-2001_10
ORD IDord-086338c2e6a64c31862edfe61a8af3d1
出典メモuspto-grants-2001_10