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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 722983Generated: October 30, 2026

Trifluoroacetic anhydride → methyl 6-chloronicotinate N-oxide

https://huagongshe.com/reaction/722983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantCarbamide PeroxideHCID 31294—
ReactantMethyl 6-chloropyridine-3-carboxylateHCID 254249—
SolventAcetonitrileHCID 6342—
Productmethyl 6-chloronicotinate N-oxideHCID 21885872104.5%

Reaction Steps

2-chloro-5-methoxycarbonylpyridine (7.0 g) and urea-hydrogen peroxide adduct (6.93 g) were suspended in acetonitrile (100 mL), and trifluoroacetic anhydride (9.92 mL) was dropwise added thereto at 0° C. The reaction mixture was stirred at room temperature for 5 hours, and evaporated in vacuo to remove the solvent. After addition of saturated aqueous sodium hydrogen carbonate and aqueous sodium thiosulfate to the residue, the mixture was extracted 5 times with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, and filtered to remove the sodium sulfate. The organic solvent was evaporated in vacuo and the resulting residue was purified by column chromatography on silica gel (hexane:ethyl acetate=2:8) to give the title compound as a pale brown solid (8.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138525B2
Source datasetuspto-grants-2006_11
ORD IDord-48057088731d4289b8636eb89a59796c
Source noteuspto-grants-2006_11