Benzyl Alcohol → 3-(Benzyloxy)-5-bromopyridine

Participants

Reaction Conditions

Reaction Steps

NaH (60% in mineral oil) (40.9 g 1.0225 mol) in 800 mL of DMF was cooled to 0° C., and benzyl alcohol (105 mL 1.014 mol) was added slowly. The reaction mixture was stirred for 1 hour at 20° C., then 3,5-dibromopyridine (200.4 g, 846 mmol) was added and the mixture was stirred for 16 hours. The mixture was quenched with saturated NH4Cl (500 mL), diluted with water and extracted with Et2O. The combined Et2O extracts were washed with 50% brine and dried (MgSO4). The solvent was evaporated in vacuo and the crude product was recrystallized from Et2O to afford the title product (161 g,72%): mp 63-68° C.; 1H NMR (CDCl3, 300 MHz) δ 8.37-8.27 (m, 2H), 7.5-7.35 (m, 6H), 5.1 (s, 1H), MS (CI/NH3) m/z 264, 266 (M+H)+.

Provenance & Evidence