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Methanol → 1-Methyl-3-n-propyl-2-iminoimidazolidin-4-one

HRID 1440765
Notes
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Reaction equation

HRID 1440765 reaction equation
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]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

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

Product 1

HCID 542389381-Methyl-3-n-propyl-2-iminoimidazolidin-4-oneYield 74.7%

Procedure

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.

Workup

  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

Sources & evidence

ORD record
ord-c08634c764ad4bdbb610fbcbf4502dd7
Source dataset
uspto-grants-1996_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05500406

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes