Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 340221Erstellt: 23. Oktober 2026

m-Chloroperbenzoic acid → 3-(benzyloxy)-5-bromopyridine N-oxide

https://huagongshe.com/de/reaction/340221

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktm-Chloroperbenzoic acidHCID 70297—
Edukt3-(Benzyloxy)-5-bromopyridineHCID 15389198—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-(benzyloxy)-5-bromopyridine N-oxideHCID 58213489—

Reaktionsschritte

A solution of 3-(benzyloxy)-5-bromopyridine (from step 1) (1.0 eq.) and meta-chloroperbenzoic acid (mCPBA) (4.0 eq.) in dichloromethane (0.1 M) was stirred at room temperature for 18 hours. The reaction was quenched with saturated aqueous NaHCO3 solution and extracted with dichloromethane three times. The combined organic layers were dried over anhydrous MgSO4 and concentrated en vacuo. The crude residue was purified by a COMBIFLASH® system (ISCO) using 0-100% ethyl acetate in hexane to give 3-(benzyloxy)-5-bromopyridine 1-oxide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08895577B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-de248117621e4c63ae8d5cb3e3b3d08a
Quellennotizuspto-grants-2014_11