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-phenyl pyridine and 40 mg (0.716 mmol) of iron powder were mixed and stirred. It was cooled to 0° C. and 4.0 g (25 mmol) of bromine was added dropwise with stirring, and watching heat generation, and it was raised to 90° C., and stirred for 10 hours. After the reaction, this reaction mixture was dissolved in chloroform to produce a solution, which was washed with 5% sodium thiosulfate aqueous solution. The chloroform solution was dried with sodium sulfate, and then concentrated. The residue was purified by silica gel column chromatography, and the desired 2-(bromophenyl)pyridine was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08492007B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-7a9e177fe2674b13aa753ee058bd7e03 |
| Source note | uspto-grants-2013_07 |