preparation | (1) preparation of 4-(3-(formyl) phenoxy) benzonitrile 122g(1mol) M-hydroxybenzaldehyde, 110 ml DMF, potassium carbonate 276g(2mol) were added to the reaction kettle, P-fluorobenzonitrile 182g(2mol) was added under stirring, reaction was carried out at ℃ for 16h, cooling, adding water, extracting with ethyl acetate for three times, recovery of ethyl acetate, methanol slurry, filtration, drying to give Brown solid 203G, yield 91%;(2) 4-(4-bromo-3-formylphenoxy) benzonitrile preparation 223G (1mol)4-(3-(formyl) phenoxy) benzonitrile, 17.2 ml of acetonitrile, 0.1g(1.1mol) of p-toluenesulfonic acid was added to the reaction kettle at 25 °c, and 196g (mol)NBS was added to the reaction kettle in batches, and refluxed for 6h, acetonitrile was recovered, water was added, filtration, methanol pulping, and drying to give a white solid of 245g, with a yield of 81%. |