Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1025609Generated: November 2, 2026

2-Bromo-6-fluorobenzaldehyde → 1-(3-bromo-2-formylphenyl)-1H-pyrazole-3-carbonitrile

https://huagongshe.com/reaction/1025609

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-6-fluorobenzaldehydeHCID 22473977—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178510229HCID 178510229—
SolventDimethyl SulfoxideHCID 679—
Product1-(3-bromo-2-formylphenyl)-1H-pyrazole-3-carbonitrileHCID 8667372073%

Reaction Steps

1H-pyrazole-3-carbonitrile (850 mg, 9.13 mmol) was dissolved in 15 mL of dry DMSO and potassium tert-butoxide (1.08 g, 9.13 mmol, Eq: 1.00) was added. The mixture was stirred at room temperature for 20 minutes and 2-bromo-6-fluorobenzaldehyde (3.71 g, 18.3 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-3-carbonitrile (1.83 g, 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729078B2
Source datasetuspto-grants-2014_05
ORD IDord-9c0e6d278a6e4fe381867c40f1e8b510
Source noteuspto-grants-2014_05