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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1259089Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1259089

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
PatentnummerUS08466167B2
Quelldatensatzuspto-grants-2013_06
ORD IDord-ffcc0f99ca19412cb283d8b33d0bbc84
Quellennotizuspto-grants-2013_06