HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1461739Erstellt: 24. Oktober 2026
Sodium Iodide → Ethyl 2-acetyl-4-[4-(4-fluorobenzoyl)piperidino]-butyrate
https://huagongshe.com/de/reaction/1461739
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Iodide | HCID 5238 | — |
| Edukt | Ethyl Acetoacetate | HCID 8868 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | Methanone, [1-(2-chloroethyl)-4-piperidinyl](4-fluorophenyl)- | HCID 10516150 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Ethyl 2-acetyl-4-[4-(4-fluorobenzoyl)piperidino]-butyrate | HCID 14882705 | — |
Reaktionsschritte
A solution of 5.45 g of ethyl acetoacetate in 20 ml of tetrahydrofuran is added at 0° C. to a suspension of 1.68 g of sodium hydride at a concentration of 60% in oil in 100 ml of anhydrous tetrahydrofuran. The medium is maintained at 20° C. for 1 hour 30 minutes. 6.3 g of sodium iodide are added, followed by the addition at 0° C. of 11.3 g of 1-(2-chloroethyl)-4-(4-fluorobenzoyl)piperidine in 100 ml of tetrahydrofuran. The reaction mixture is brought to reflux for 15 hours. It is concentrated under vacuum. The residue is taken up in water and the product is extracted with dichloromethane.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US05077288 |
|---|
| Quelldatensatz | uspto-grants-1991_12 |
|---|
| ORD ID | ord-eb99b06868674e2c9d29b38620f253b3 |
|---|
| Quellennotiz | uspto-grants-1991_12 |
|---|