Реакция #2554

Уравнение реакции

4-(4-fluorobenzoyl)-1-(2-hydroxyethyl)piperidine

DMF

thionyl chloride

→

title compound

Выход 96.3%

1-(2-Chloroethyl)-4-(4-fluorobenzoyl)piperidine hydrochloride

Выход 96.3%

Растворители

methylene chloride

Условия реакции

Обработка

1. 1
   Температураwith cooling in an ice bath
2. 2
   Другоеthe solvent was removed by evaporation
3. 3
   workup.DISTILLATIONthe resulting residue was subjected to azeotropic distillation
4. 4
   ПромывкаThereafter, the thus obtained residue was washed with an ether-methylene chloride (4:1) mixture solution (30 ml)

Методика

In an atmosphere of dry air, 4-(4-fluorobenzoyl)-1-(2-hydroxyethyl)piperidine (1.96 g, 7.8 mmol) was dissolved in methylene chloride (10 ml) to which, with cooling in an ice bath, were subsequently added dropwise DMF (0.1 ml) and thionyl chloride (2.5 ml, 34.2 mmol). After 7 hours of stirring at room temperature, the solvent was removed by evaporation, and the resulting residue was subjected to azeotropic distillation using benzene (15 ml×2). Thereafter, the thus obtained residue was washed with an ether-methylene chloride (4:1) mixture solution (30 ml) to obtain 2.3 g (96.3%) of the title compound in the form of light beige powder.

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