HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1084328Generated: November 1, 2026
2,4-Dimethylpyridine → 5-Bromo-2,4-dimethylpyridine
https://huagongshe.com/reaction/1084328
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4-Dimethylpyridine | HCID 7936 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Fuming sulfuric acid | HCID 24681 | — |
| Product | 5-Bromo-2,4-dimethylpyridine | HCID 13411100 | — |
| Product | 3-Bromo-2,4-dimethylpyridine | HCID 14003064 | — |
Reaction Steps
150 ml of 65% strength oleum are added dropwise to 28.9 ml of 2,4-dimethylpyridine, while cooling with ice and stirring, such that the temperature does not rise above 35° C. When the solution has become homogeneous, 6.42 ml of bromine are slowly added dropwise, with stirring. The mixture is stirred at 80° C. for 31/2 hours. After cooling, it is carefully added dropwise to 1 kg of ice, neutralized with solid Na2CO3 and extracted 3 times with 300 ml of ether each time. The organic layer is separated off and dried over magnesium sulfate. After removal of the solvent by distillation in vacuo, 34.6 g of a pale yellow oil consisting of the isomers 5-bromo-2,4-dimethylpyridine and 3-bromo-2,4-dimethylpyridine are obtained. The isomers are separated by column chromatography on silicon dioxide gel to give 10 g of 5-bromo-2,4-dimethylpyridine as a colorless liquid (13.0 g of 3-bromo-2,4-dimethylpyridine).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05004748 |
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| Source dataset | uspto-grants-1991_04 |
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| ORD ID | ord-1b250b7748c64548840c6339ce197675 |
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| Source note | uspto-grants-1991_04 |
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