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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943754Generated: November 1, 2026

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

https://huagongshe.com/reaction/1943754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantHCID 178526735HCID 178526735—
CatalystBenzyltrimethylammonium chlorideHCID 5963—
SolventAcetonitrileHCID 6342—
Product2-Chloro-5-fluoro-3-nitropyridineHCID 1077362670%

Reaction Conditions

Temperature80 °C

Reaction Steps

5-fluoro-3-nitro-pyridin-2-ol (2 g, 12.7 mmol) and benzyltrimethyl ammonium chloride (1.17 g, 6.35 mmol) were dissolved in acetonitrile, and phosphorus oxychloride (3.5 ml, 38.1 mmol) was added thereto and stirred at 80° C. 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:methanol=30:1. The fractions containing the product were collected and evaporated to obtain yellow liquid (1.57 g, 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394792B2
Source datasetuspto-grants-2013_03
ORD IDord-0abad51d7529491d864ff7a7237f3854
Source noteuspto-grants-2013_03