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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1687Erstellt: 23. Oktober 2026

m-Chloroperbenzoic acid → 2-ethyl-3-chloromethylpyridine-N-oxide

https://huagongshe.com/de/reaction/1687

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktm-Chloroperbenzoic acidHCID 70297—
Edukt3-(chloromethyl)-2-ethylPyridineHCID 19690958—
LösungsmittelChloroformHCID 6212—
Produkt2-ethyl-3-chloromethylpyridine-N-oxideHCID 19690998—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

The 2-ethyl-3-chloromethylpyridine (2.4 g, 15.4 mmol) was dissolved in CHCl3 (100 mL) and cooled under nitrogen to 0° C. and m-chloroperbenzoic acid (55%, 4.2 g) was added in small portions. The reaction was stirred for 2 hours. The reaction was extracted twice with saturated aqueous sodium bicarbonate (100 mL). The organic phase was dried with MgSO4, filtered and the solvent was removed under reduced pressure. The residue was chromatographed on silica gel packed in 98:2 CH2Cl2 :MeOH and eluted with the same. The appropriate fractions were combined and the solvent removed under reduced pressure the give the desired 2-ethyl-3-chloromethylpyridine-N-oxide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05726172
Quelldatensatzuspto-grants-1998_03
ORD IDord-50b5f885709f4236b5aee536d764bea9
Quellennotizuspto-grants-1998_03