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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333068Generated: October 30, 2026

m-Chloroperbenzoic acid → 2-Chloro-6-methylpyridine 1-oxide

https://huagongshe.com/reaction/333068

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant6-Chloro-2-picolineHCID 87601—
SolventDichloromethaneHCID 6344—
Product2-Chloro-6-methylpyridine 1-oxideHCID 4579772—

Reaction Conditions

Temperature40 °C

Reaction Steps

2-Chloro-6-methylpyridine (12.76 g, 0.1 mol) was dissolved together with m-chloroperbenzoic acid (17.56 g, 0.15 mol) in DCM (100 ml) and stirred at 40° C. for 90 minutes. The heating bath was removed and stirring was continued overnight at room temperature. The reaction mixture was quenched with saturated sodium thiosulfate solution and the pH was adjusted to 8 with 1M NaOH. The phases were separated, the aqueous phase extracted with DCM and the combined organic phases were dried over magnesium sulfate. The solvent was removed under reduced pressure and unreacted 2-chloro-6-methylpyridine was removed by distillation (2 mbar, 65° C.). 2-Chloro-6-methyl-pyridine 1-oxide was obtained as residue (6.0 g of a yellow oil, 0.042 mol, 42%). MS (ESI) m/z=144.0 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877934B2
Source datasetuspto-grants-2014_11
ORD IDord-8324e3b058454acab71c208d7548a50b
Source noteuspto-grants-2014_11