Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427263Generated: October 31, 2026

Azobisisobutyronitrile → 2-(Bromomethyl)-6-fluoropyridine

https://huagongshe.com/reaction/2427263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantHexaneHCID 8058—
ReactantN-bromobutanimideHCID 67184—
Reactant2-Fluoro-6-methylpyridineHCID 96090—
SolventEthyl AcetateHCID 8857—
Product2-(Bromomethyl)-6-fluoropyridineHCID 13985218—

Reaction Conditions

Temperature65 °C

Reaction Steps

Add NBS (35.6 g, 0.20 mole) to a solution of 6-fluoro-2-methylpyridine (20 mL, 0.19 mole) in EtOAc (400 mL) at room temperature. When the temperature reaches 45° C., add AIBN (400 mg, 2.4 mmol). Heat the mixture at 65° C. for 6 h, then cool to room temperature and add hexane (1 L). Remove the white precipitate by filtration and wash the solid with hexane/EtOAc (1:1). Wash the filtrate with small amounts of aqueous Na2S2O3, NaHCO3, and brine. Dry the organics (Na2SO4), filter, then remove most of the solvent under vacuum at room temperature. Transfer the remaining solution to a distillation set-up. Remove the remaining solvent by distilling at atmospheric pressure, followed by the unreacted starting material at 80 mm (bp ca 70° C.; 11.2 g) and then the title product at 1 mm (bp ca 75° C.; 12.1 g, 32%). NMR (300 MHz; CDCl3): 7.82 (1H; dd); 7.35 (1H; dd); 6.90 (1H; dd); 4.50 (2H; s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968587B2
Source datasetuspto-grants-2011_06
ORD IDord-965146ba5115477bbbd329ced55b5460
Source noteuspto-grants-2011_06