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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243875Generated: October 26, 2026

Sodium Bicarbonate → 3-fluoro-2-(1H-pyrazol-5-yl)benzonitrile

https://huagongshe.com/reaction/243875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant2-Bromo-3-fluorobenzonitrileHCID 2783393—
Reactant1H-Pyrazole-5-boronic acidHCID 11251979—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product3-fluoro-2-(1H-pyrazol-5-yl)benzonitrileHCID 6711692820.7%

Reaction Conditions

Temperature23 °C

Reaction Steps

2-Bromo-3-fluorobenzonitrile (1.0 g, 5.0 mmol) and (1H-pyrazol-5-yl)boronic acid (647 mg, 4.6 mmol) were combined and dissolved in degassed DME (15 mL) then treated with NaHCO3 (1260 mg, 8.4 mmol) in water and the reaction purged with bubbling N2 for 5 minutes. The reaction was treated with Pd(PPh3)4 (288 mg, 0.2 mmol) and then purged with bubbling for 5 minutes in a sealed vessel and then heated to reflux for 2 h. The reaction was then cooled to 23° C. filtered and the solids were rinsed with EtOAc and the layers separated. The organic layers were combined, dried and concentrated under reduced pressure. Chromatography (0-30% ethyl acatate/hexanes) afforded 3-fluoro-2-(1H-pyrazol-5-yl)benzonitrile (178 mg, 19%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653263B2
Source datasetuspto-grants-2014_02
ORD IDord-a08601227d3d4cc4a757065d38125524
Source noteuspto-grants-2014_02