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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 261471Erstellt: 26. Oktober 2026

1-Benzyl-4-piperidone → 1-Benzyl-4-(4-chloro-2-fluorobenzyl)-4-piperidinol

https://huagongshe.com/reaction/261471

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Benzyl-4-piperidoneHCID 19220—
Edukt4-Chloro-2-fluorobenzyl bromideHCID 2736551—
Produkt1-Benzyl-4-(4-chloro-2-fluorobenzyl)-4-piperidinolHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04166120
Quelldatensatzuspto-grants-1979_08
ORD IDord-76b6b9eba4444415be73c093dc853d61
Quellennotizuspto-grants-1979_08