HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 899988Generated: November 4, 2026
Acetic Acid → 2-Bromo-4-(bromomethyl)pyridine
https://huagongshe.com/reaction/899988
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Bromo-4-methylpyridine | HCID 2734087 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 2-Bromo-4-(bromomethyl)pyridine | HCID 12954806 | 28.3% |
Reaction Steps
0.073 ml of acetic acid is added to a solution of 0.172 g of 2-bromo-4-methylpyridine in 2.5 ml of carbon tetrachloride, under an inert atmosphere of argon at a temperature in the region of 20° C. The mixture brought, with stirring, to a temperature of 50° C. 0.356 g of N-bromosuccinimide and 0.048 g of benzoyl peroxide are added successively at this temperature. The mixture is maintained at 80° C. for about 18 hours. After cooling, the reaction medium is placed on a cartridge 20 mm in diameter packed with 10 g of 20-40 μm silica not conditioned beforehand, and then eluted with dichloromethane at a flow rate of 5 ml/minute. The fractions between 30 and 40 ml are concentrated to dryness under reduced pressure. 0.071 g of 2-bromo-4-(bromomethyl)pyridine is thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07354933B2 |
|---|
| Source dataset | uspto-grants-2008_04 |
|---|
| ORD ID | ord-228773cad6b54e8986dea8ee8544a588 |
|---|
| Source note | uspto-grants-2008_04 |
|---|