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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant4,6-Dibromo-2-(2,4-difluorophenyl)-3-methylpyridineHCID 22648039—
SolventCarbon TetrachlorideHCID 5943—
Product4,6-Dibromo-3-(bromomethyl)-2-(2,4-difluorophenyl)pyridineHCID 22648117—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06809199B2
Source datasetuspto-grants-2004_10
ORD IDord-8c9e8154d86c4d20b1a5188c8134d260
Source noteuspto-grants-2004_10