HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Carbonate → 2,6-Dibromopyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2,6-Dibromopyridine | HCID 12274 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2,6-Dibromopyridine | HCID 12274 | — |
| Product | 2,6-Diphenylpyridine | HCID 72920 | — |
| Product | 2-Bromo-6-phenylpyridine | HCID 568679 | — |
Reaction Steps
To a mixture of 600 mg (2.5 mmol) of 2,6-dibromopyridine in 15 mL of toluene was added a mixture of 150 mg (1.27 mmol) of phenylboronic acid in 5 mL of methanol, 86 mg (0.075 mmol) of Pd(PPh3)4 and 15 mL of 2 M Na2CO3. The mixture was refluxed overnight, cooled, extracted with ethyl acetate, dried and 2-bromo-6-phenylpyridine isolated chromatographically from unreacted 2,6-dibromopyridine and 2,6-diphenylpyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07256186B2 |
| Source dataset | uspto-grants-2007_08 |
| ORD ID | ord-3451a2226e724a519ba58f4c3cb38d4d |
| Source note | uspto-grants-2007_08 |