HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Phenylpyridine → 2-(2-Bromophenyl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Phenylpyridine | HCID 13887 | — |
| Reactant | Bromine | HCID 24408 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-(2-Bromophenyl)pyridine | HCID 13223929 | 35.4% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
3 g (19.3 mmol) of 2-phenylpyridine and 40 mg (0.716 mmol) of an iron powder were mixed and stirred. 4.0 g (25 mmol) of bromine was dropped paying attention to heat generation while stirring and cooling the mixture to 0° C., and the mixture was heated up to 90° C. and stirred for 10 hours. After completion of the reaction, this reaction mixture was dissolved in chloroform, and washed with a 5% aqueous sodium thiosulfate solution. The chloroform solution was dried over sodium sulfate, then, concentrated, and the residue was purified by silica gel column chromatography, to obtain the intended 2-(bromophenyl)pyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07947340B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-66625216ddc04b3990b0170475934285 |
| Source note | uspto-grants-2011_05 |