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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943748Generated: November 2, 2026

Phosphorus oxychloride → 2-Chloro-5-methyl-3-nitropyridine

https://huagongshe.com/reaction/1943748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantHCID 178430719HCID 178430719—
CatalystBenzyltrimethylammonium chlorideHCID 5963—
SolventAcetonitrileHCID 6342—
Product2-Chloro-5-methyl-3-nitropyridineHCID 81830097%

Reaction Steps

5-methyl-3-nitro-pyridin-2-ol (5 g, 32.4 mmol) and benzyltrimethyl ammonium chloride (3.01 g, 16.2 mmol) were dissolved in acetonitrile, and phosphorus oxychloride (9.0 ml, 97.2 mmol) was added thereto and stirred at 800 for 6 hours. The reaction mixture was cooled and poured into ice water to quench the reaction, and extracted with dichloromethane. The combined organic layer was washed with saturated saline solution, dried over anhydrous sodium sulfate (Na2SO4), filtered and evaporated under reduced pressure. The residue was purified by column chromatography on silica eluting with a solvent of dichloromethane. The fractions containing the product were collected and evaporated to obtain 2-chloro-5-methyl-3-nitro-pyridine as yellow solid (5.39 g, 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394792B2
Source datasetuspto-grants-2013_03
ORD IDord-c2ff4a311979427c82e72970c4596d9b
Source noteuspto-grants-2013_03