HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 612355Erstellt: 24. Oktober 2026
Acetic Acid → (4-Hydroxyimino-cyclohexa-2,5-dienylidene)-thiophen-2-yl-acetonitrile
https://huagongshe.com/de/reaction/612355
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Nitrobenzene | HCID 7416 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | 2-Thienylacetonitrile | HCID 72880 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | (4-Hydroxyimino-cyclohexa-2,5-dienylidene)-thiophen-2-yl-acetonitrile | HCID 19594042 | 50,2% |
Reaktionsschritte
9.5 g of KOH are dissolved in 50 ml of methanol. To the solution are added 5 g (41 mmol) of thiophene-2-acetonitrile followed by 4.2 ml (41 mmol) of nitrobenzene. After the reaction mixture is stirred at room temperature for 2 hrs, 200 ml of water are added with stirring. The resulting solution is acidified by addition of 30 ml of acetic acid in 25 ml of water, leading to a dark orange precipitate. The mixture is then filtered, and the solid is washed with a mixture of methanol and water, and methanol. The crude product is dried in air and recrystallized from toluene. 4.7 g (50%) of (4-Hydroxyimino-cyclohexa-2,5-dienylidene)-thiophen-2-yl-acetonitrile are obtained in the form of a dark orange powder having a melting point of 151-155° C. (dec.).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US06004724 |
|---|
| Quelldatensatz | uspto-grants-1999_12 |
|---|
| ORD ID | ord-56fa11f9501247e99ec0bf6f2fefe14b |
|---|
| Quellennotiz | uspto-grants-1999_12 |
|---|