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Piperazine → 1-(Cyclopropylcarbonyl)piperazine Hydrochloride

HRID 886986
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 886986
[NH:1]1[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1.[CH:7]1([C:10]([Cl:12])=[O:11])[CH2:9][CH2:8]1>C(O)(=O)C>[ClH:12].[CH:7]1([C:10]([N:1]2[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]2)=[O:11])[CH2:9][CH2:8]1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 4837PiperazineHCID 77637Cyclopropanecarbonyl chloride

Produkt 1

HCID 208479551-(Cyclopropylcarbonyl)piperazine Hydrochloride

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 176Acetic AcidLösungsmittel

Reaktionsbedingungen

Temperatur
40 °C

Versuchsvorschrift

Acetic acid (700 ml) was treated with piperazine (50.00 g, 0.581 mol) portionwise over 15 minutes with stirring under nitrogen The reaction mixture was warmed to 40° C. and maintained at this temperature until a complete solution was obtained. Cyclopropanecarbonyl chloride 59.2 ml, 0.638 mol) was added over 15 minutes. The reaction mixture was stirred at room temperature overnight. The reaction mixture was filtered and the filtrate distilled under reduced pressure until ˜430 ml of distillates had been collected. Toluene (550 ml) was charged to the reaction mixture and reduced pressure distillation continued until a further 400 ml of distillates were collected. A further charge of toluene (550 ml) was added and reduced pressure distillation continued until 350 ml of distillates were collected. The resulting slurry was diluted with toluene (200 ml) and stirred overnight. Further toluene (500 ml) was added in order to mobilise the slurry. The slurry was filtered, washed with toluene (100 ml) and dried in vacuo at 40° C. to give the title compound as an off white solid (86.78 g).

Aufarbeitung

  1. temperaturemaintained at this temperature until a complete solution
  2. customwas obtained
  3. stirringThe reaction mixture was stirred at room temperature overnight
  4. filtrationThe reaction mixture was filtered
  5. distillationthe filtrate distilled under reduced pressure until ˜430 ml of distillates
  6. customhad been collected
  7. additionToluene (550 ml) was charged to the reaction mixture and reduced pressure distillation
  8. customwere collected
  9. additionA further charge of toluene (550 ml)
  10. additionwas added
  11. distillationreduced pressure distillation
  12. customwere collected
  13. additionThe resulting slurry was diluted with toluene (200 ml)
  14. stirringstirred overnight
  15. additionFurther toluene (500 ml) was added in order
  16. filtrationThe slurry was filtered
  17. washwashed with toluene (100 ml)
  18. customdried in vacuo at 40° C.

Quellen und Nachweise

ORD-Eintrag
ord-ff77e54d95304e5aacc56e34b41de24c
Quelldatensatz
uspto-grants-2012_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08247416B2

Notizen zur Reaktion

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