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Methyl iodide → HCID 178456402, compound

HRID 2305309
Notes
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Reaction equation

HRID 2305309 reaction equation
[CH:1](=[N:8][N:9]1[CH2:13][CH2:12][N:11]([CH2:14][CH2:15][CH3:16])[C:10]1=NC)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C[I:20].[C:21](#[N:23])C>>[I-:20].[CH:1](=[N:8][N:9]1[CH2:13][CH2:12][N:11]([CH2:14][CH2:15][CH3:16])[C:10]1=[CH:21][NH3+:23])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 6328Methyl iodideHCID 6342AcetonitrileHCID 542477831-Benzylideneamino-2-methylimino-3-propyl-imidazolidine

Product 1

HCID 178456402HCID 178456402, compound

Procedure

A mixture of 0.51 g of 1-benzylideneamino-2-methylimino-3-propyl-imidazolidine in 15 ml of acetonitrile with 0.36 g of methyliodide is refluxed for ca. one hour and the solvent is evaporated off. The residue is treated with acetonitrile and the solvent is evaporated off. (1-benzylideneamino-3-propyl-imdazolidine-2-yliden)methyl-ammonium iodide is obtained in the form of a powder.

Workup

  1. temperatureis refluxed for ca. one hour
  • customthe solvent is evaporated off
  • additionThe residue is treated with acetonitrile
  • customthe solvent is evaporated off
  • Sources & evidence

    ORD record
    ord-22593d6d99b341f3823de4f7a6223122
    Source dataset
    uspto-grants-2002_08
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US06440957B1

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes