HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

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

HRID 2293036
Notes
Print preview

Reaction equation

HRID 2293036 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-223b29e7c8a34940934cb553c4a61ccb
Source dataset
uspto-grants-1997_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05686390

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes