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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050707Generated: October 31, 2026

Potassium Carbonate → 2-(pyridin-4-yl)-2H-benzo[d][1,2,3]triazole

https://huagongshe.com/reaction/1050707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chloropyridinium hydrochlorideHCID 22117864—
ReactantHCID 178418385HCID 178418385—
SolventDimethylformamideHCID 6228—
Product2-(pyridin-4-yl)-2H-benzo[d][1,2,3]triazoleHCID 6413440—

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 4-chloropyridinium hydrochloride (25.0 g, 166 mmol), benzotriazole (29.6 g, 249 mmol), potassium carbonate (69.1 g, 500 mmol), and dimethylformamide (DMF) (500 mL) was stirred and heated under argon at 130° C. for 3 days. After cooling, the solid was filtered off, and the solvent was evaporated under reduced pressure. The residue was treated with dichloromethane (200 mL), filtered and chromatographed using a column filled with silica gel (500 mL) and hexane/ethyl acetate (1:1) as an eluent. Fractions containing the desired product were combined, and the solvent was distilled off. The residue was triturated with ethanol, the solid was filtered off and dried in a vacuum oven to give 2-(pyridin-4-yl)-2H-benzo[d][1,2,3]triazole, 6.45 g, 20%). 1H NMR (400 MHz, CDCl3): δ 8.80 (m, 2H, pyridine), 8.26 (m, 2H, pyridine), 7.93 (m, 2H, benzotriazole), 7.46 (m, 2H, benzotriazole).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382424B2
Source datasetuspto-grants-2016_07
ORD IDord-92a9f68b69cf4b9f9b05d9384e5c55b8
Source noteuspto-grants-2016_07