Benzyl Bromide → 1-(Benzyloxy)-2-fluoro-4-nitrobenzene

Participants

Reaction Steps

A mixture of 2-fluoro-4-nitrophenol (15 g, 95.5 mmol) and benzyl bromide (18 g, 105 mmol) in acetone (125 ml) containing potassium carbonate (26.5 g, 190 mmol) was refluxed for 2 hours. The volatiles were removed and the residue was partitioned between 2N hydrochloric acid and ethyl acetate. The organic layer was separated, washed with water, brine, dried (MgSO4) and the volatiles were removed under vacuum. The solid was triturated with petroleum ether to give 2-fluoro-4-nitro-benzyloxybenzene (23 g, 97%).

Provenance & Evidence