Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410122Generated: October 31, 2026

Methyl iodide → 5-Chloro-1-methyl-3-nitropyridin-2-one

https://huagongshe.com/reaction/2410122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178526657HCID 178526657—
SolventDimethylformamideHCID 6228—
Product5-Chloro-1-methyl-3-nitropyridin-2-oneHCID 86703119—

Reaction Conditions

Temperature5 °C

Reaction Steps

A mixture of NaH (577 mg, 14.4 mmol) and 5-chloro-2-hydroxy-3-nitropyridine (2.1 g, 12.0 mmol) in DMF (21 mL) was stirred for 1 h at 5° C. Methyl iodide (1.1 mL, 18.0 mmol) was added. The resulting mixture was allowed to warm to rt, stirred overnight, cooled to 0° C., quenched by addition of water, and extracted with EtOAc. The organic layer was dried (Na2SO4), filtered, and concentrated. The residue was used without further purification. tR: 0.61 min (LC-MS 2); ESI-MS: 189.1/191.1 [M+H]+ (LC-MS 2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815926B2
Source datasetuspto-grants-2014_08
ORD IDord-de86455240f14e0db4e69d55d7d77106
Source noteuspto-grants-2014_08