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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2120316Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/2120316

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktEthyl AcetateHCID 8857—
EduktThionyl ChlorideHCID 24386—
Edukt2-Propenoic acid, 3-(4-nitrophenyl)-HCID 70156—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-(4-nitrophenyl)prop-2-enoyl ChlorideHCID 31946399,2%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06689899B2
Quelldatensatzuspto-grants-2004_02
ORD IDord-fdb31367611f40619b8ef82bc1701b31
Quellennotizuspto-grants-2004_02