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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509377Generated: October 30, 2026

Acetonitrile → methyl 6-chloronicotinate N-oxide

https://huagongshe.com/reaction/509377

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantCarbamide PeroxideHCID 31294—
ReactantMethyl 6-chloropyridine-3-carboxylateHCID 254249—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Productmethyl 6-chloronicotinate N-oxideHCID 21885872—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 500 mL round bottom flask containing methyl 6-chloronicotinate (4.50 g, 26.2 mmol) was added MeCN (100 mL). The resulting mixture was then stirred at 0° C. for 10 min. At this time, urea hydrogen peroxide (4.93 g, 52.5 mmol) solid was added before the dropwise addition of trifluoroacetic anhydride (7.41 mL, 52.5 mmol). The reaction was stirred for 30 min and then the ice bath was removed. The reaction was then stirred for 3 h and then the bulk of MeCN was removed by rotary evaporation. The residue was dissolved in EtOAc (150 mL) and washed with sodium thiosulfate (aqueous, 0.5 M, 2×100 mL), water (100 mL), brine (100 mL), dried with sodium sulfate and concentrated to a tan solid. The solid thus obtained was dissolved in DCM (150 mL) and MeOH (30 mL). The solid residue was removed by filtration, and the filtrate was concentrated affording 2-chloro-5-(methoxycarbonyl)pyridine 1-oxide as a tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096527B2
Source datasetuspto-grants-2015_08
ORD IDord-3f7c1e2a2b8d49f09fa0465e51b14230
Source noteuspto-grants-2015_08