HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Ethyl cyanoacetate → Ethyl 3-(2-chlorophenyl)-2-cyanobut-2-enoate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Ethyl cyanoacetate | HCID 7764 | — |
| Edukt | Ethanone, 1-(2-chlorophenyl)- | HCID 72864 | — |
| Edukt | Ammonium Acetate | HCID 517165 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | Ethyl 3-(2-chlorophenyl)-2-cyanobut-2-enoate | HCID 67073569 | — |
Reaktionsschritte
A mixture of 2′-chloroacetophenone (50 mmol), ethyl cyanoacetate (50 mmol), acetic acid (1.14 mL) ammonium acetate (400 mg), and benzene (50 mL) is heated to reflux in a Dean-Stark apparatus. After approximately hours, additional ethyl cyanoacetate (50 mmol), acetic acid (1.14 mL), and ammonium acetate (400 mg) are added. After an additional 10 hours, the reaction is cooled to room temperature, diluted with ethyl acetate (30 mL), washed with water (240 mL), brine (40 mL), and dried (Na2SO4). After filtering, the extract is concentrated in vacuo and the desired product, as a mixture of E and Z-isomers, is isolated by column chromatography on silica gel, eluting with 5% ethyl acetate in petroleum ether.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07449490B2 |
| Quelldatensatz | uspto-grants-2008_11 |
| ORD ID | ord-fd54da5602114e94950de7957523fde0 |
| Quellennotiz | uspto-grants-2008_11 |