HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
1-Benzyl-4-piperidone → 1-Benzyl-4-(4-chloro-2-fluorobenzyl)-4-piperidinol
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 1-Benzyl-4-piperidone | HCID 19220 | — |
| Edukt | 4-Chloro-2-fluorobenzyl bromide | HCID 2736551 | — |
| Produkt | 1-Benzyl-4-(4-chloro-2-fluorobenzyl)-4-piperidinol | HCID 12733222 | — |
Reaktionsschritte
A sample of 4-chloro-2-fluorobenzyl bromide is converted to its Grignard reagent which is reacted with N-benzyl-4-piperidone to provide 1-benzyl-4-(4-chloro-2-fluorobenzyl)-4-piperidinol. The above is performed in a manner consistent with the procedure of Example 2A. This product is distilled at 175°-180° C., 0.18 mm to provide an orange oil which is converted in ether to its hydrogen chloride salt. The salt is recrystallized four times from an ethyl alcohol-ether mixture to provide the purified salt, m.p. 211.5°-213° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04166120 |
| Quelldatensatz | uspto-grants-1979_08 |
| ORD ID | ord-76b6b9eba4444415be73c093dc853d61 |
| Quellennotiz | uspto-grants-1979_08 |