HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121314Generated: November 4, 2026
2-Phenylpyridine → 2-(2-Bromophenyl)pyridine
https://huagongshe.com/reaction/2121314
Participants
| Role | Name | HCID | Charge |
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| 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 Steps
2-Phenylpyridine 3 g(19.3 mmol) and iron powder 40 mg(0.716 mmol) were mixed and stirred. Bromine 4.0 g (25 mmol) was added dropwise with stirring at 0° C., avoiding the rising temperature. Then the mixture was heated up to 90° C. and keep the temperature for ten hours with stirring. After the completion of the reaction, this reaction mixture was dissolved into chloroform solution and washed with 5% aqueous sodium thiosulfate solution. After dried by sodium sulufate, the organic solution was concentrated by an evaporator. The residue obtainedwas purifiedbyuse of silica gel column chromatography. 1.6 g (6.83 mmol) of 2-(bromophenyl)pyridine was obtained and the yield was 35.4%. Analysis: M+=234.0 By FD-MS.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06696180B2 |
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| Source dataset | uspto-grants-2004_02 |
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| ORD ID | ord-2e2663cb402a498e9c71ffccaeb94064 |
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| Source note | uspto-grants-2004_02 |
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