HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Piperidine → (3Z)-6-Chloro-3-[(3-chloro-2-fluorophenyl)methylidene]-1,3-dihydro-2H-indol-2-one
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Piperidine | HCID 8082 | — |
| Edukt | 3-Chloro-2-fluorobenzaldehyde | HCID 736335 | — |
| Edukt | 6-Chloro-1,3-dihydroindol-2-one | HCID 736344 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | (3Z)-6-Chloro-3-[(3-chloro-2-fluorophenyl)methylidene]-1,3-dihydro-2H-indol-2-one | HCID 71464325 | 89% |
Reaktionsbedingungen
| Temperatur | 50 °C |
|---|
Reaktionsschritte
To the mixture of 6-chloro-2-oxindole (11 g, 65.6 mmol) (Crescent) and 3-chloro-2-fluorobenzaldehyde (12 g, 75.7 mmol) (Aldrich) in methanol (140 mL) was added piperidine (5.59 g, 65.6 mmol) (Aldrich) dropwise. The mixture was then heated at 50° C. for 3 h. After cooled to 4° C., the mixture was filtered and resulting precipitate was collected, dried to give E/Z-6-chloro-3-(3-chloro-2-fluoro-benzylidene)-1,3-dihydro-indol-2-one as a yellow solid (Yield 18 g, 89%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08217044B2 |
| Quelldatensatz | uspto-grants-2012_07 |
| ORD ID | ord-c0f1046dc2af44be8808bc44c8217a53 |
| Quellennotiz | uspto-grants-2012_07 |