HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 380723Erstellt: 26. Oktober 2026
Hydrochloric Acid → 3-(4-nitrophenyl)prop-2-enoyl Chloride
https://huagongshe.com/reaction/380723
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | Thionyl Chloride | HCID 24386 | — |
| Edukt | 2-Propenoic acid, 3-(4-nitrophenyl)- | HCID 70156 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 3-(4-nitrophenyl)prop-2-enoyl Chloride | HCID 319463 | 99,2% |
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 mixture, the reaction mixture was refluxed with stirring until the generation of hydrogen chloride gas stopped. The reacted solution was concentrated until a solid could be precipitated and then poured into hexane. The precipitated solid was separated by filtration and dried. 210 g of 4-nitrocinnamoyl chloride was yielded. 63.5 g (0.3 mole) of 4nitrocinnamoyl chloride and 400 g of methylethylketone were placed in a reaction vessel and the reaction mixtures were stirred by heating at 50° C. under a nitrogen current. 15.42 g (0.14 mole) of resorcinol, 32 g of pyridine, and 100 g of methylethylketone were added dropwise to the above reaction vessel using a dropping funnel. After the completion of the addition, the reaction solution was refluxed with stirring under a nitrogen current for 2 hours. After the reaction, the precipitate was separated by filtration and the filtrated solid was washed by water and dried. 64 g of white colored crystals (1,3-bis(4-nitrocinnamic acid) benzene) was yielded.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06303742B1 |
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| Quelldatensatz | uspto-grants-2001_10 |
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| ORD ID | ord-5003da8c5d184c6ab6a738b1a8524c3d |
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| Quellennotiz | uspto-grants-2001_10 |
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