HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 394167Generated: October 30, 2026
Benzoyl Peroxide → 4,6-Dibromo-3-(bromomethyl)-2-(2,4-difluorophenyl)pyridine
https://huagongshe.com/reaction/394167
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4,6-Dibromo-2-(2,4-difluorophenyl)-3-methylpyridine | HCID 22648039 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 4,6-Dibromo-3-(bromomethyl)-2-(2,4-difluorophenyl)pyridine | HCID 22648117 | — |
Reaction Steps
To a stirred solution of 4,6-dibromo-2-(2,4-difluorophenyl)-3-methylpyridine (5.0 g, 13.77 mmol, 1 eq) in CCl4 (125 mL) was added N-bromosuccinimide (2.95 g, 16.6 mmol 1.2 eq) and benzoyl peroxide (340 mg, 1.37 mmol, 0.1 eq). The mixture was brought to and maintained at reflux until all the starting material was consumed (approx 3.5 h). The reaction mixture was cooled to 0° C. and the succinimide was filtered off. The solvent was removed under reduced pressure and the product was purified by flash column chromatography on silica gel elufing with 2% Et2O in hexanes giving 4,6-dibromo-3-(bromomethyl)-2-(2,4-difluorophenyl)pyridine. Mass spectrum (ESI) 440.1 (M+1); 442.1 (M+3); 444.1 (M+5); 446.1 (M+7). 1H NMR (500 MHz, CDCl3) δCHCl3: 7.84 (1H, s); 7.50 (1H, m); 7.05 (1H, m); 6.96 (1H, m); 4.44 (2H br s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06809199B2 |
|---|
| Source dataset | uspto-grants-2004_10 |
|---|
| ORD ID | ord-8c9e8154d86c4d20b1a5188c8134d260 |
|---|
| Source note | uspto-grants-2004_10 |
|---|