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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1059966Generated: October 26, 2026

Nitric Acid → 1-Chloro-4-(4-methoxypyridin-2-yl)-2-nitrobenzene

https://huagongshe.com/reaction/1059966

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantSodium BicarbonateHCID 516892—
Reactant4-(4-Methoxypyridin-2-yl)-chlorobenzeneHCID 18631015—
SolventSulfuric AcidHCID 1118—
Product1-Chloro-4-(4-methoxypyridin-2-yl)-2-nitrobenzeneHCID 18667563—

Reaction Conditions

Temperature5 °C

Reaction Steps

To a suspension of 4-(4-methoxypyridin-2-yl)chlorobenzene (500 mg) in sulfuric acid (4 ml) was added fuming nitric acid (0.2 ml) dropwise at 0° C., and the mixture was stirred at 5° C. for 30 minutes. The reaction mixture was poured into a saturated aqueous sodium hydrogencarbonate solution and extracted with ethyl acetate. The separated organic layer was washed with water and brine, dried over sodium sulfate and evaporated under reduced pressure. The residue was triturated with diisopropyl ether, filtered, washed with diisopropyl ether and dried under reduced pressure to give 1-chloro-4-(4-methoxypyridin-2-yl)-2-nitrobenzene (601 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06521643B1
Source datasetuspto-grants-2003_02
ORD IDord-111a1b45b6f54895952c275907f26941
Source noteuspto-grants-2003_02