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1,3-Propanediamine, N1,N1,N3-trimethyl- → HCID 16109013, compound

HRID 1042694
Notes
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Reaction equation

HRID 1042694 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5](F)=[C:4]([N+:9]([O-:11])=[O:10])[CH:3]=1.[CH3:12][N:13]([CH3:19])[CH2:14][CH2:15][CH2:16][NH:17][CH3:18]>>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([N:17]([CH3:18])[CH2:16][CH2:15][CH2:14][N:13]([CH3:19])[CH3:12])=[C:4]([N+:9]([O-:11])=[O:10])[CH:3]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 783021,3-Propanediamine, N1,N1,N3-trimethyl-HCID 27363284-Bromo-1-fluoro-2-nitrobenzene

Product 1

HCID 16109013HCID 16109013, compound

Procedure

To a round bottom flask at 0° C. was added 4-Bromo-1-fluoro-2-nitrobenzene (10 g, 45.46 mmol) and N,N,N′-Trimethyl-propane-1,3-diamine (6.99 ml, 47.73 mmol). The reaction was allowed to warm to RT and stirred for 16 h. The reaction was extracted into EtOAc, washed once with saturated aqueous NaHCO3, twice with water, and then dried over Mg2SO4. The organic layer was filtered and concentrated to yield the title compound as a bright orange solid.

Workup

  1. extractionThe reaction was extracted into EtOAc
  2. washwashed once with saturated aqueous NaHCO3, twice with water
  3. dry with materialdried over Mg2SO4
  4. filtration
The organic layer was filtered
  • concentrationconcentrated
  • Sources & evidence

    ORD record
    ord-a9fccb10f35a42358339b8bd56120457
    Source dataset
    uspto-grants-2013_10
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US08557996B2

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes