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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867893Generated: October 30, 2026

Potassium Carbonate → 5-Bromo-2-chloro-4-(4-chlorophenyl)pyridine

https://huagongshe.com/reaction/1867893

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chlorophenylboronic acidHCID 74299—
Reactant5-Bromo-2-chloro-4-iodopyridineHCID 21865140—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
Product5-Bromo-2-chloro-4-(4-chlorophenyl)pyridineHCID 5797973770.7%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a degassed solution of 5-bromo-2-chloro-4-iodopyridine (Ref. Cottet, F. and Schlosser, M. Tetrahedron 60, 11896-11874 (2004)) (2.0 g, 6.3 mmol), 4-chlorophenylboronic acid (1.1 g, 6.9 mmol) and K2CO3 (1.7 g, 12.6 mmol) in 1,2-dimethoxyethane (24 mL) and H20 (8.0 mL) was added Pd(PPh3)4 (0.727 g, 0.63 mmol) under argon at 20° C. The reaction mixture was refluxed for 15 h under argon, then allowed to cool to 20° C. The reaction was quenched by addition of H2O (30 mL) and extracted with EtOAc (50 mL×3). The combined organic was washed with saturated aqueous NaHCO3 (50 mL) and saturated aqueous NaCl (50 mL), dried over MgSO4, filtered and concentrated in vacuo. The residue was crystallized in EtOH to afford 1.35 g of the title compound as a light beige solid as the first crop. The second crop of the title product (0.44 g) was also isolated by concentrating the mother liquid followed by recrystallization in EtOH. LC/MS (method B): retention time=2.03 min, [M+H]+=301.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07632837B2
Source datasetuspto-grants-2009_12
ORD IDord-533f174aba15436bb66b850522e59808
Source noteuspto-grants-2009_12