HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493391Generated: October 25, 2026
Toluene → 5-Bromo-2-(2-methylphenyl)pyridine
https://huagongshe.com/reaction/493391
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | 5-Bromo-2-iodopyridine | HCID 593690 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Product | 5-Bromo-2-(2-methylphenyl)pyridine | HCID 13128385 | 84% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07534763B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-a0b31f3e6ee643148705b086bce46969 |
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| Source note | uspto-grants-2009_05 |
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