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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172293Generated: October 30, 2026

Potassium Carbonate → 4-(2-Bromo-5-(trifluoromethyl)phenyl)pyridine

https://huagongshe.com/reaction/2172293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(Pyridin-4-yl)boronic acidHCID 2734379—
Reactant1-Bromo-2-iodo-4-(trifluoromethyl)benzeneHCID 46735231—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product4-(2-Bromo-5-(trifluoromethyl)phenyl)pyridineHCID 8668734041.4%

Reaction Conditions

Temperature120 °C

Reaction Steps

A solution of pd(ph3p)4 (1.410 g, 1.220 mmol), 1-bromo-2-iodo-4-(trifluoromethyl)benzene (3.94 ml, 24.41 mmol), pyridin-4-ylboronic acid (3.00 g, 24.41 mmol), and potassium carbonate (13.49 g, 98 mmol) in 32 mL dioxane and 6 mL water was heated to 120° C. overnight. Additional portions of pyridin-4-ylboronic acid (3.00 g, 24.41 mmol) and potassium carbonate (13.49 g, 98 mmol) were added and the reaction mixture was heated to 120° C. for 3 hours. The reaction mixture was then poured into water and was extracted with DCM. The organics were then concentrated. Purification of the crude residue by silica gel column chromatography (0-100% EtOAc/heptane) gave 4-(2-bromo-5-(trifluoromethyl)phenyl)pyridine (3.054 g, 10.11 mmol, 41.4% yield) as a white solid. [M+H]+=303.9

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051311B2
Source datasetuspto-grants-2015_06
ORD IDord-0160cba926f14d01886ae1c13f15487d
Source noteuspto-grants-2015_06