HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598104Generated: October 30, 2026
2,6-Dibromopyridine → 2-Bromo-6-(2,4,6-trimethylphenyl)pyridine
https://huagongshe.com/reaction/598104
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Dibromopyridine | HCID 12274 | — |
| Reactant | 2,4,6-Trimethylbenzeneboronic acid | HCID 292184 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 2-Bromo-6-(2,4,6-trimethylphenyl)pyridine | HCID 71413697 | 68% |
Reaction Steps
2,6-Dibromopyridine (9.47 g, 40 mmol) was dissolved in 80 mL of 1,2-dimethoxyethane (1,2-dimethoxyethane). Tetrakis(triphenylphosphine)palladium(0) (2.31 g, 2.00 mmol) was added and the mixture was heated at 50° C. for 15 min. The solution was cooled and 2,4,6-trimethylbenzeneboronic acid (6.56 g, 40 mmol) dissolved in 40 mL of 1,2 dimethoxyethane was added. Finally, potassium t-butoxide (8.97 g, 80 mmol) was added as a solution in 40 mL of t-butanol. The reaction was heated for 0.5 h at 90° C. The solution was cooled and filtered through celite. Flash chromatography (2% ethyl acetate/hexanes) gave 7.48 g (68% yield) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07897607B2 |
|---|
| Source dataset | uspto-grants-2011_03 |
|---|
| ORD ID | ord-2783704e0ed34a58819241a63fb9a129 |
|---|
| Source note | uspto-grants-2011_03 |
|---|