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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1427449Generated: November 1, 2026

Potassium Carbonate → 5-Nitro-2-(4-(trifluoromethyl)phenyl)pyridine

https://huagongshe.com/reaction/1427449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-DioxaneHCID 31275—
Reactant2-Chloro-5-nitropyridineHCID 78308—
Reactant4-(Trifluoromethyl)phenylboronic acidHCID 2734389—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
Product5-Nitro-2-(4-(trifluoromethyl)phenyl)pyridineHCID 6798085137%

Reaction Conditions

Temperature80 °C

Reaction Steps

4-(trifluoromethyl)phenylboronic acid (500 mg, 2.63 mmol), 2-chloro-5-nitropyridine (417 mg, 2.63 mmol), potassium carbonate (908 mg, 6.58 mmol) and palladium(II) acetate (23.6 mg, 0.105 mmol) were combined in 1:1 dioxane:water (10 mL). The resulting mixture was stirred at 80° C. for 12 hours. The mixture was filtered and the solution was extracted with ethyl acetate. The organic layer was washed with water, then brine, dried over sodium sulfate, filtered and concentrated. Purification by column chromatography gave 5-nitro-2-(4-(trifluoromethyl)phenyl)pyridine (260 mg, 37%). 1H NMR (400 MHz, CDCl3, δ): 9.47 (s, 1H), 8.51 (d, 1H), 8.14 (d, 2H), 7.72 (d, 1H), 7.65 (d, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933104B2
Source datasetuspto-grants-2015_01
ORD IDord-581300d2d8c040a7a29bff58f8313c41
Source noteuspto-grants-2015_01