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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534036Generated: October 26, 2026

Acetonitrile → 5-bromo-3-(1-ethyl-1H-pyrazol-5-yloxy)picolinonitrile

https://huagongshe.com/reaction/534036

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantSodium CarbonateHCID 10340—
Reactant5-Bromo-3-nitropyridine-2-carbonitrileHCID 2769698—
ReactantHCID 178418331HCID 178418331—
SolventEthyl acetate chloroform hexaneHCID 22239056—
Product5-bromo-3-(1-ethyl-1H-pyrazol-5-yloxy)picolinonitrileHCID 6748583253.3%

Reaction Steps

5-Bromo-3-nitropicolinonitrile (24.0 g, 105 mmol), 1-ethyl-1H-pyrazol-5-ol (13.0 g, 116 mmol), and sodium carbonate (11.2 g, 105 mmol) were combined with acetonitrile (400 ml). The mixture was heated to reflux for 20 hours, then cooled to ambient temperature, filtered and evaporated. The residue was dissolved in ethyl acetate (800 ml) and washed with water (3×200 ml) and brine, dried (MgSO4), filtered and evaporated. The crude material was purified over silica gel (15:35:50, then 20:30:50 ethyl acetate/chloroform/hexane) to afford 5-bromo-3-(1-ethyl-1H-pyrazol-5-yloxy)picolinonitrile (16.4 g, 53% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853409B2
Source datasetuspto-grants-2014_10
ORD IDord-ee3ea7d408464061a8ba91aa00effe88
Source noteuspto-grants-2014_10