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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1524935Generated: October 31, 2026

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

https://huagongshe.com/reaction/1524935

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 acetate/hexanes) afforded 3-fluoro-2-(1H-pyrazol-5-yl)benzonitrile (178 mg, 19%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079911B2
Source datasetuspto-grants-2015_07
ORD IDord-c6f22b7c8b1b4e209d191569375b9759
Source noteuspto-grants-2015_07