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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1025613Generated: October 27, 2026

1H-Pyrazole-4-carbonitrile → 1-(3-bromo-2-formylphenyl)-1H-pyrazole-4-carbonitrile

https://huagongshe.com/reaction/1025613

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Pyrazole-4-carbonitrileHCID 564449—
Reactant2-Bromo-6-fluorobenzaldehydeHCID 22473977—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
Product1-(3-bromo-2-formylphenyl)-1H-pyrazole-4-carbonitrileHCID 8667372255.4%

Reaction Steps

1H-pyrazole-4-carbonitrile (935 mg, 10.0 mmol, Eq: 1.00) was dissolved in 15 mL of dry DMSO and potassium tert-butoxide (1.19 g, 10.0 mmol, Eq: 1.00) was added. The mixture was stirred at room temperature for 20 minutes and 2-bromo-6-fluorobenzaldehyde (4.08 g, 20.1 mmol, Eq: 2) was added. The mixture was stirred at room temperature overnight and then extracted with ethyl acetate and water. The organic layer was dried and concentrated. The crude material was purified by flash chromatography (silica gel, 40 g, 20% to 40% EtOAc in hexanes) to give 1-(3-bromo-2-formylphenyl)-1H-pyrazole-4-carbonitrile (1.53 g, 55%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729078B2
Source datasetuspto-grants-2014_05
ORD IDord-1b1df8405c7e4ab285cb26745765008d
Source noteuspto-grants-2014_05