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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1156037Erstellt: 25. Oktober 2026

m-Chloroperbenzoic acid → 1-Methyl-4-phenoxy-4-phenylpiperidine N-oxide

https://huagongshe.com/reaction/1156037

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktm-Chloroperbenzoic acidHCID 70297—
EduktPiperidine, 1-methyl-4-phenoxy-4-phenyl-HCID 3060394—
LösungsmittelMethanolHCID 887—
Produkt1-Methyl-4-phenoxy-4-phenylpiperidine N-oxideHCID 53888329—

Reaktionsschritte

1.5 g of 1-methyl-4-phenoxy-4-phenylpiperidine are dissolved in 4 ml of methanol, and 1.7 g of 80% strength m-chloroperbenzoic acid, dissolved in methanol, are added slowly thereto while cooling with ice. After stirring the mixture at room temperature for 3 hours, the solvent is stripped off and the residue is partitioned between concentrated sodium hydroxide solution and chloroform. The crude N-oxide hydrate (which remains after drying the chloroform phase and evaporating off the solvent) is taken up in a little methanol, and the equivalent amount of methanolic fumaric acid is added. 1 g of a colorless precipitate is obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04333942
Quelldatensatzuspto-grants-1982_06
ORD IDord-73c031d5a4e942119bc30554cd4ce55d
Quellennotizuspto-grants-1982_06