Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360692Generated: November 1, 2026

Ethanol → 2-(4-Bromo-2,6-difluorobenzyl)-6-(2,4-difluorophenyl)pyridine

https://huagongshe.com/reaction/1360692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
Reactant2,4-Difluorophenylboronic acidHCID 2734334—
Reactant2-Bromo-6-(4-bromo-2,6-difluorobenzyl)pyridineHCID 57700371—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product2-(4-Bromo-2,6-difluorobenzyl)-6-(2,4-difluorophenyl)pyridineHCID 5770036688.9%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 2-bromo-6-(4-bromo-2,6-difluorobenzyl)pyridine (from Step C above, 7.41 g, 20.53 mmol) in toluene (200 mL) was added (2,4-difluorophenyl)boronic acid (3.89 g, 24.63 mmol), tetrakis(triphenylphosphine)palladium (2.37 g, 2.05 mmol), ethanol (20 mL) and 2M Na2CO3 (20 mL). The reaction was heated to 90° C. until complete. The mixture was cooled to room temperature and concentrated. The crude residue was diluted with EtOAc/water (1:1) and washed with 1N HCl (2×), brine (3×), dried over MgSO4, and concentrated in vacuo. The crude material was purified via silica gel chromatography (hexanes/ethyl acetate) to give the title compound (7.23 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879875B2
Source datasetuspto-grants-2011_02
ORD IDord-482ddb4600564ed49432b5d08b7aae13
Source noteuspto-grants-2011_02