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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220252Generated: October 25, 2026

Toluene → 5-Bromo-2-(2-methylphenyl)pyridine

https://huagongshe.com/reaction/2220252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant5-Bromo-2-iodopyridineHCID 593690—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventSodium CarbonateHCID 10340—
Product5-Bromo-2-(2-methylphenyl)pyridineHCID 1312838584%

Reaction Steps

To an argon-purged and evacuated slurry of 910 mg (3.21 mmol) of 5-bromo-2-iodopyridine and 436 mg (3.21 mmol, 1.0 eq.) of 2-o-tolylboronic acid in 8 mL of toluene and 3.2 mL of 2 M aqueous sodium carbonate, was added 36 mg (0.032 mmol, 0.01 eq) of tetrakis(triphenylphosphine) palladium. The reaction mixture was purged and evacuated with argon twice more and then set to reflux under argon for 15 h. The reaction was cooled and partitioned between water and EtOAc. The layers were separated, and the aqueous layer extracted once more with EtOAc. The organic extracts were combined, dried over magnesium sulfate, filtered, concentrated and dried in vacuo to give the crude product as an orange oil. Purification by silica gel chromatography (7:3 CH2Cl2/hexanes) provided the title compound as a yellow oil, 666 mg, 84% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417028B2
Source datasetuspto-grants-2008_08
ORD IDord-11b7b240fac34c139fa4e1a44b7f1622
Source noteuspto-grants-2008_08