Reacción #219170

Ecuación de reacción

piperidine hydrochloride

hydrochloric acid

calcium chloride

4-methylpropiophenone

1,3-dioxolane

→

Tolperisone Hydrochloride

Condiciones de reacción

Tratamiento posterior

1. 1
   LavadoThe powder in the funnel is washed afterwards with 20 ml 1,3-dioxolane
2. 2
   OtroThe reaction mixture is purged once with argon
3. 3
   workup.DISSOLUTIONThe white precipitate dissolves after approximately 15-16 hours
4. 4
   workup.WAITAfter 24 hours the heating is switched off
5. 5
   Otrothe oil bath is removed
6. 6
   Temperaturawhile still warm
7. 7
   workup.STIRRINGunder vigorous stirring to the clear reaction solution, there
8. 8
   workup.ADDITIONis added 800 ml ethyl acetate
9. 9
   Temperaturathe solution is cooled to ambient temperature
10. 10
    workup.ADDITIONfurther treated with 400 ml methyl tert-butylether (MTBE)
11. 11
    workup.STIRRINGThe resulting precipitate is agitated at α to 10° C. for an additional 2 hours
12. 12
    Filtraciónfiltered off over a glass
13. 13
    Filtraciónfilter (Po-3)
14. 14
    Lavadowashed afterwards twice with 200 ml MTBE each time
15. 15
    OtroThe substance is dried in the vacuum
16. 16
    Otrodrying oven at 75-80° C.
17. 17
    workup.WAIT20-40 mbar for 16 to 24 hours

Procedimiento

In a 3-L-three neck flask with a reflux condenser, a calcium chloride drying tower, and under an argon flow, 200 ml of 1,3-dioxolane and 146.2 ml of 4-methylpropiophenone are subjected to agitation and then there is added through a funnel 100 g piperidine hydrochloride and 4.0 ml of 33% aqueous hydrochloric acid. The powder in the funnel is washed afterwards with 20 ml 1,3-dioxolane, and the stirrer is switched on in the reaction flask. The reaction mixture is purged once with argon and stirred at 100-105° C. bath temperature (83-86° C. interior temperature). The white precipitate dissolves after approximately 15-16 hours. After 18-20 hours the thin layer chromatogram shows no more piperidine. After 24 hours the heating is switched off and the oil bath is removed and while still warm, and under vigorous stirring to the clear reaction solution, there is added 800 ml ethyl acetate and then the solution is cooled to ambient temperature and then further treated with 400 ml methyl tert-butylether (MTBE). The resulting precipitate is agitated at α to 10° C. for an additional 2 hours, and then filtered off over a glass filter (Po-3) and washed afterwards twice with 200 ml MTBE each time. The substance is dried in the vacuum drying oven at 75-80° C. and 20-40 mbar for 16 to 24 hours.

Fuente