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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120317Generated: October 26, 2026

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

https://huagongshe.com/reaction/2120317

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrophenolHCID 980—
ReactantPyridineHCID 1049—
Reactant3-(4-nitrophenyl)prop-2-enoyl ChlorideHCID 319463—
SolventAcetoneHCID 180—
Product(4'-Nitrophenyl)-4-nitrocinnamateHCID 5371111395.5%

Reaction Conditions

Temperature50 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06689899B2
Source datasetuspto-grants-2004_02
ORD IDord-4e8fc877538341dc85e53ac69f21d830
Source noteuspto-grants-2004_02