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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1687Generated: October 25, 2026

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

https://huagongshe.com/reaction/1687

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant3-(chloromethyl)-2-ethylPyridineHCID 19690958—
SolventChloroformHCID 6212—
Product2-ethyl-3-chloromethylpyridine-N-oxideHCID 19690998—

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05726172
Source datasetuspto-grants-1998_03
ORD IDord-50b5f885709f4236b5aee536d764bea9
Source noteuspto-grants-1998_03