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llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
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Methanol → 1-Methyl-3-n-propyl-2-iminoimidazolidin-4-one

HRID 2293036
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2293036
I.[CH3:2][N:3]1[CH2:7][C:6](=[O:8])[N:5]([CH2:9][CH2:10][CH3:11])[C:4]1=[NH:12].CO.[OH-].[K+]>>[CH3:2][N:3]1[CH2:7][C:6](=[O:8])[N:5]([CH2:9][CH2:10][CH3:11])[C:4]1=[NH:12]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 887MethanolHCID 14797Potassium HydroxideHCID 676185061-Methyl-3-n-propyl-2-iminoimidazolidin-4-one hydroiodide

Produkt 1

HCID 542389381-Methyl-3-n-propyl-2-iminoimidazolidin-4-oneAusbeute 74,7 %

Versuchsvorschrift

2.83 g (10 mmol) of the 1-methyl-3-n-propyl-2-iminoimidazolidin-4-one hydroiodide was added to 25 ml of methanol containing 0.66 g (10 mmol) of 85% potassium hydroxide, and the mixture was stirred at room temperature for one hour. Methanol was distilled off under reduced pressure, and chloroform was added to the residue. Precipitated crystals were removed by filtration. Chloroform was distilled off under reduced pressure to obtain 1.16 g of 1-methyl-3-n-propyl-2-iminoimidazolidin-4-one as an oily substance.

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Aufarbeitung

  1. distillationMethanol was distilled off under reduced pressure, and chloroform
  2. additionwas added to the residue
  3. customPrecipitated crystals
  4. customwere removed by filtration
  5. distillationChloroform was distilled off under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-223b29e7c8a34940934cb553c4a61ccb
Quelldatensatz
uspto-grants-1997_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05686390

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