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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733192Generated: October 30, 2026

4-Bromo-1-methoxy-2-(trifluoromethyl)benzene → 4-(4-Methoxy-3-(trifluoromethyl)phenyl)-6-propylpyrimidine-2-carbonitrile

https://huagongshe.com/reaction/733192

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-1-methoxy-2-(trifluoromethyl)benzeneHCID 2775304—
Reactant4-Propyl-6-trimethylstannanyl-pyrimidine-2-carbonitrileHCID 69049300—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
Product4-(4-Methoxy-3-(trifluoromethyl)phenyl)-6-propylpyrimidine-2-carbonitrileHCID 4986247211.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

Bis(triphenylphosphine)palladium dichloride (34 mg, 0.05 mmol) was added under a nitrogen atmosphere to a mixture of 4-propyl-6-trimethylstannanyl-pyrimidine-2-carbonitrile (150 mg, 0.48 mmol) and 4-methoxy-3-trifluoromethyl-bromobenzene (148 mg, 0.58 mmol) in dimethylformamide (3 mL). The mixture was heated for 5 hours at 80° C. then concentrated under reduced pressure. The residue was partitioned between ethyl acetate and water. The aqueous layer was extracted twice with ethyl acetate. The combined organic layers were concentrated under reduced pressure. The residue was chromatographed over silica gel (eluent Cyclohexane/DCM 7/3) to afford a solid which was triturated in pentane. After filtration, 4-(4-methoxy-3-trifluoromethyl-phenyl)-6-propyl-pyrimidine-2-carbonitrile (18 mg, 11%) was obtained as an off white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07589095B2
Source datasetuspto-grants-2009_09
ORD IDord-a9d80b6fad584e33b7f31fdd07669c47
Source noteuspto-grants-2009_09