반응 #219170

ord-d216d59b83b949c5b5bf552e7fcd8c9b

반응 방정식

C1CCNCC1.Cl
piperidine hydrochloride
Cl
hydrochloric acid
[Ca+2].[Cl-].[Cl-]
calcium chloride
CCC(=O)c1ccc(C)cc1
4-methylpropiophenone
C1COCO1
1,3-dioxolane
Cc1ccc(C(=O)C(C)CN2CCCCC2)cc1.Cl
Tolperisone Hydrochloride

반응 조건

온도
84.5°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    세척The powder in the funnel is washed afterwards with 20 ml 1,3-dioxolane
  2. 2
    기타The 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
    기타the oil bath is removed
  6. 6
    온도while 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
    온도the 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
    여과filtered off over a glass
  13. 13
    여과filter (Po-3)
  14. 14
    세척washed afterwards twice with 200 ml MTBE each time
  15. 15
    기타The substance is dried in the vacuum
  16. 16
    기타drying oven at 75-80° C.
  17. 17
    workup.WAIT20-40 mbar for 16 to 24 hours

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07385060B2uspto-grants-2008_06