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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860387Generated: November 1, 2026

2,6-Lutidine → 2,6-Dimethylpyridine N-oxide

https://huagongshe.com/reaction/1860387

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-LutidineHCID 7937—
ReactantSodium SulfateHCID 24436—
Reactantm-Chloroperbenzoic acidHCID 70297—
SolventDichloromethaneHCID 6344—
Product2,6-Dimethylpyridine N-oxideHCID 14083—

Reaction Steps

Sodium sulphate (6 g) and a solution of m-chloroperbenzoic acid (40 g) in DCM (140 ml) was added to a solution of 2,6-lutidine (5 ml) in dry DCM (60 ml). The mixture was stirred at 23° and under a nitrogen atmosphere for 18 h; then it was quenched with a saturated aqueous sodium bicarbonate solution (200 ml). Then a solution of potassium carbonate was added and the aqueous phase was saturated with NaCl and then it was extract with DCM (3×100 ml). The organic extract was dried and concentrated in vacuo to a yellow oil which was purified by flash chromatography (eluting in gradient from EA to EA-MeOH 9:1) to give the title compound as a yellow oil (4.7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06531466B2
Source datasetuspto-grants-2003_03
ORD IDord-e21c929b0d0547f09663b0a11b70155e
Source noteuspto-grants-2003_03