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Ethanol → HCID 19907417, compound

HRID 2371520
Notes
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Reaction equation

HRID 2371520 reaction equation
[CH2:1]([N:3]([CH2:21][CH3:22])[CH2:4][CH2:5][CH2:6][C:7]1[CH:12]=[CH:11][C:10]([CH2:13][CH2:14][CH2:15][N:16]([CH2:19][CH3:20])[CH2:17][CH3:18])=[CH:9][CH:8]=1)[CH3:2].[CH2:23]([I:25])[CH3:24].[CH2:26](O)[CH3:27]>>[I-:25].[I-:25].[CH2:19]([N+:16]([CH2:23][CH3:24])([CH2:17][CH3:18])[CH2:15][CH2:14][CH2:13][C:10]1[CH:9]=[CH:8][C:7]([CH2:6][CH2:5][CH2:4][N+:3]([CH2:26][CH3:27])([CH2:1][CH3:2])[CH2:21][CH3:22])=[CH:12][CH:11]=1)[CH3:20]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 702EthanolHCID 6340IodoethaneHCID 199073731,4-Bis(3-diethylaminopropyl)benzene

Product 1

HCID 19907417HCID 19907417, compound

Procedure

304 mg of 1,4-bis(3-diethylaminopropyl)benzene was dissolved in 2.5 ml of absolute ethanol, and after dropwise addition of 1.56 g of ethyl iodide, the mixture was refluxed for 1.5 hours in dark. After cooling, ethanol was partially removed under reduced pressure, the resulting crystal was filtered, quickly washed with ethanol and dried in vacuo to obtain 461 mg of the title compound as a colorless crystal.

Workup

  1. temperaturethe mixture was refluxed for 1.5 hours in dark
  • temperatureAfter cooling
  • customethanol was partially removed under reduced pressure
  • filtrationthe resulting crystal was filtered
  • washquickly washed with ethanol
  • customdried in vacuo
  • Sources & evidence

    ORD record
    ord-f56d38cc919b4907a66efe008234e97d
    Source dataset
    uspto-grants-1992_03
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US05093370

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes