Benzoyl (CAS NO.: ), with other names like Piperidine, 1-benzoyl-, could be produced through the following synthetic methods.

In a 5-l., two-necked, round-bottomed flask, fitted with an efficient reflux condenser, is placed a mixture of 130 g. (131 cc., 1.64 moles) of dry pyridine and 3 l. of absolute alcohol. During the course of forty to fifty minutes 450 g. (19.6 atoms) of sodium is added gradually. The sodium is added in as large pieces as can be inserted through the second opening in the flask. One and one-half liters of absolute alcohol is now added and the mixture heated over an oil bath for two to three hours until the sodium disappears. It is desirable not to allow the reaction mixture to cool at this point but to separate the piperidine immediately. The condenser is set for distillation and a separatory funnel is inserted through the stopper in the second opening of the flask. The alcohol is then distilled using an oil bath. The addition of a piece of zinc facilitates an even distillation. During this procedure, water to the amount of 1700–1800 cc. is added to the reaction mixture through the separatory funnel, slowly at first and later as rapidly as possible. At the beginning, this addition must be very cautious as the heat evolved causes a very distillation of alcohol. After about 200 cc. of water has been added, the mixture begins to solidify and remains semi-solid until most of the water has been added. The distillation is continued until practically all the alcohol has distilled (three to four hours). At the end of this time there remains in the distilling flask about 1500 cc. of residue, which is discarded. The distillate is about 5 l. in volume. To this is added 200 cc. of concentrated hydrochloric acid (sp. gr. 1.19) and the mixture is then returned to the distilling flask. The alcohol is removed by distillation on a steam bath until the residual volume in the flask amounts to about 600–800 cc.; this requires two to three hours.

The residue is then transferred to a 2-l. round-bottomed flask fitted with a mechanical stirrer and separatory funnel. The mixture is treated with stirring with a solution of 186 g. of technical sodium hydroxide or 170 g. (4.25 moles) of c.p. sodium hydroxide in about 300 cc. of water. With continuous stirring 235 g. (1.67 moles) of benzoyl chloride is now added during the course of one hour, keeping the temperature down by cooling with running water. After the addition, the reaction mixture is cooled, the amide separated, washed with a little water and distilled under reduced pressure. The product boils at 180–184° /20 mm., 191–194° /27 mm., 240–244° /130 mm., and weighs 240–250 g. (77–81 per cent of the theoretical amount).

Benzoyl piperidine thus obtained is a straw-colored viscous liquid. Upon long standing or seeding with crystalline benzoyl piperidine, the compound crystallizes in long, colorless needles which melt at 44°. The literature reports 48° as the melting point of the pure material.

Using 180 g. of pyridine in place of the 130 g. suggested, and a corresponding increase in the other chemicals except the sodium and alcohol, a yield of 300–326 g. of benzoyl piperidine is obtained. This is a smaller percentage yield (70–75 per cent of the theoretical amount) but the actual yield more than repays for the excess of pyridine used.