Parapenzolate bromide

Chemical Name N-Methyl-4-piperidylbenzilate methobromide Common Name — [Pg.1164]

N-methyl-4-piperidvl benzi/ata and the methiodide An intimate mixture of 0.1 mol of N-methyM-piperidinol hydrochloride and 0.1 mol diphenylchloroacetyl chloride is heated at 160°C to 180°C until the evolution of hydrogen chloride ceases (usually about 4 to 5 hours). The melt is then dissolved in 500 ml of water and the resultant mixture heated on a steam bath for about Vi hour, after which time complete solution is effected. The acid solution is cooled and rendered alkaline with ammonium hydroxide solution whereupon the ester is precipitated.The ester is purified either by removal by filtration and recrystallization from benzene petroleum ether or by extracting the mixture with benzene and precipitating the ester by the addition of petroleum ether. After recrystallization there is obtained about 0.06 mol of N-methyl-4-piperidyl benzilate, melting point 1 62°C to 163°C. [Pg.1164]

To a solution of 0.05 mol of the above-obtained ester in about 100 ml of anhydrous benzene there are added 15 ml of methyl iodide. The ensuing mixture is refluxed for several hours whereupon the quaternary salt is deposited and removed by filtration. Recrystallization from ethanol or ethanol-ether yields the quaternary salt, melting point 199°C to 200°C. [Pg.1164]

N-methyl-4-piperidyl benzilate methobromide To a suspension of 0.15 mol of freshly prepared silver bromide in 300 ml of anhydrous methanol is added a solution of 0.1 mol of quaternary iodide obtained as above. The mixture is stirred and refluxed for several hours after which time transhalogenation is complete. The mixture is cooled, the insoluble silver [Pg.1164]

British Patent 788,126 December 23,1957 assigned to Schering Corp. [Pg.1165]

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