HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Thiazolidinedione → 5-(4-Chlorobenzylidene)-2,4-thiazolidinedione
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Thiazolidinedione | HCID 5437 | — |
| Edukt | 4-Chlorobenzaldehyde | HCID 7726 | — |
| Edukt | Piperidine | HCID 8082 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 5-(4-Chlorobenzylidene)-2,4-thiazolidinedione | HCID 233070 | 43,4% |
Reaktionsschritte
To a solution of 20 g (171 mmol) of 2,4-thiazolidinedione and 17.4 ml (171 mmol) of 4-chlorobenzaldehyde in 350 ml of ethanol, 1.68 ml (17.1 mmol) of piperidine was added, and the mixture was heated under reflux for 5 hours. After cooling, the precipitated crystals were filtered and washed with cooled ethanol to give 17.75 g of the desired compound (43.4% yield, pale yellow crystals).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05767121 |
| Quelldatensatz | uspto-grants-1998_06 |
| ORD ID | ord-8640849b69ac42fc9173ca6e5bbd63fe |
| Quellennotiz | uspto-grants-1998_06 |