HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Indole-2-carboxaldehyde → 6-chloro-3-(1H-indol-2-ylmethylene)-1,3-dihydroindol-2-one
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Indole-2-carboxaldehyde | HCID 96389 | — |
| Edukt | 6-Chloro-1,3-dihydroindol-2-one | HCID 736344 | — |
| Katalysator | Piperidine | HCID 8082 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 6-chloro-3-(1H-indol-2-ylmethylene)-1,3-dihydroindol-2-one | HCID 54553499 | 87% |
Reaktionsschritte
A mixture of 6-chloro-2-oxindole (41 mg) (commercially available), indole-2-carbaldehyde (42 mg) (prepared according to Synthetic Communications, 1993, 23, 3109) and piperidine (1 drop) in ethanol (3 mL) was held in a sealed tube at 95° C. for 3 hours. The mixture was cooled to room temperature. The solid was collected by vacuum filtration, washed with cold ethanol and dried in vacuum oven to give 62 mg (87% yield) of 6-chloro-3-(1H-indol-2-ylmethylene)-1,3-dihydroindol-2-one as a shiny orange solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06855730B2 |
| Quelldatensatz | uspto-grants-2005_02 |
| ORD ID | ord-1e89f92e0b244e2aaec6e141d1a75b76 |
| Quellennotiz | uspto-grants-2005_02 |