HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Indole-5-carboxaldehyde → 4-(2-hydroxy-ethyl)-3-(1H-indol-5-ylmethylene)-1,3-dihydro-indol-2-one
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Indole-5-carboxaldehyde | HCID 589040 | — |
| Edukt | 4-(2-Hydroxyethyl)indolin-2-one | HCID 10943004 | — |
| Katalysator | Piperidine | HCID 8082 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 4-(2-hydroxy-ethyl)-3-(1H-indol-5-ylmethylene)-1,3-dihydro-indol-2-one | HCID 53902607 | 72% |
Reaktionsbedingungen
| Temperatur | 90 °C |
|---|
Reaktionsschritte
A mixture of 4-(2-hydroxy-ethyl)-1,3-dihydro-indol-2-one (39 mg, 0.22 mmol), 1H-indole-5-carbaldehyde (32 mg, 0.22 mmol) and 1 drop of piperidine in ethanol was heated at 90° C. for overnight and cooled to room temperature. The reaction mixture was concentrated and the residue was purified on silica gel column to give 48 mg (72%) of 4-(2-hydroxy-ethyl)-3-(1H-indol-5-ylmethylene)-1,3-dihydro-indol-2-one as a yellow solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06689806B1 |
| Quelldatensatz | uspto-grants-2004_02 |
| ORD ID | ord-1ac0011f53ee44f88004f1ed02f52447 |
| Quellennotiz | uspto-grants-2004_02 |