Methyl p-acetylbenzoate (CAS NO.: ), with other names as , p-acetyl-, , could be produced through the following synthetic routes.

A 200-ml. three-necked flask is equipped with a thermometer, a mechanical stirrer, a gas inlet tube extending as far into the flask as the stirrer permits, and a trap (designed to return the heavier layer of the condensate) which is attached to a bulb and a coil-type reflux condenser connected in series. Methyl p-ethylbenzoate (98 g., 0.6 mole) and a mixture of 1 g. of chromium oxide and 4 g. of calcium carbonate, prepared by grinding the solids together in a mortar, are added. An air line with a bleed control valve is connected from the top of the condenser to a water aspirator. The flask is heated with a hemispherical electric mantle.

The mixture is stirred vigorously at a temperature of 140–150°, and air is drawn through it. for 24 hours while the water formed is collected in the trap. At the end of this period, the mixture is cooled, diluted with 100 ml. of benzene, and filtered with suction to remove the catalyst. The catalyst is washed with 10 ml. of benzene on the funnel, and the washings are combined with the filtrate. The benzene is distilled from the clear, yellow solution (conveniently at a pressure of 100 mm. or lower to avoid superheating and partial decomposition of the product) through a fractionating column. After removal of the benzene, the pressure is reduced and the residue is fractionally distilled. There is obtained 29–32 g. of unreacted methyl p-ethylbenzoate (b.p. 118–121°/16 mm.), and 43–45 g. (40–42% conversion and 60% yield) of methyl p-acetylbenzoate; b.p. 149–150°/7 mm. The high-boiling residue weighs 13–18 g. The crude methyl p-acetylbenzoate can be purified by crystallization from the minimum amount of 1:1 benzene-commercial hexane required for solution with a recovery of 82–85%, collected in two crops; m.p. 92–95°.