Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2422365Generated: October 25, 2026

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

https://huagongshe.com/reaction/2422365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant5-Bromo-2-iodopyridineHCID 593690—
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(tri-phenylphosphine)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 numberUS07960349B2
Source datasetuspto-grants-2011_06
ORD IDord-003644a08a6941fc996b0a6fc87abc19
Source noteuspto-grants-2011_06