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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193127Generated: November 2, 2026

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

https://huagongshe.com/reaction/1193127

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. Cooled to 23° C. filtered and solid 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 numberUS08680275B2
Source datasetuspto-grants-2014_03
ORD IDord-326028f97fa34fb0add83e55efb1b126
Source noteuspto-grants-2014_03