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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DimethylpyridineHCID 7936—
ReactantSodium CarbonateHCID 10340—
ReactantBromineHCID 24408—
ReactantFuming sulfuric acidHCID 24681—
Product5-Bromo-2,4-dimethylpyridineHCID 13411100—
Product3-Bromo-2,4-dimethylpyridineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05004748
Source datasetuspto-grants-1991_04
ORD IDord-1b250b7748c64548840c6339ce197675
Source noteuspto-grants-1991_04