HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Acetic Acid → Ethyl 3-(4-aminophenyl)-2-cyanoacrylate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Ethyl cyanoacetate | HCID 7764 | — |
| Edukt | Diethylamine | HCID 8021 | — |
| Edukt | 4-Aminobenzaldehyde | HCID 11158 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | Ethyl 3-(4-aminophenyl)-2-cyanoacrylate | HCID 3540149 | 83,1% |
Reaktionsschritte
36 g (0.3 mol) of para-aminobenzaldehyde are suspended in 300 ml of ethanol. 33.9 g (0.3 mol) of ethyl cyanoacetate and a mixture of 0.375 ml of diethylamine and 1.125 ml of acetic acid, as catalyst, are added to the suspension. The reaction mixture is refluxed for 2 hours, left to cool and then crystallized. After separating out the crystals by filtration and drying, 53.9 g (83% yield) of ethyl 3-(4-aminophenyl)-2-cyanoacrylate are obtained in the form of orange-coloured crystals.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07390916B2 |
| Quelldatensatz | uspto-grants-2008_06 |
| ORD ID | ord-6fe060502bb841b5a49f1768c8a4f508 |
| Quellennotiz | uspto-grants-2008_06 |