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1,8-Dibromododecane → 12-Bromododecylphthalimide

HRID 1463809
Notes
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Reaction equation

HRID 1463809 reaction equation
[C:1]1(=[O:11])[NH:5][C:4](=[O:6])[C:3]2=[CH:7][CH:8]=[CH:9][CH:10]=[C:2]12.[K].[Br:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH:21](Br)[CH2:22][CH2:23][CH2:24][CH3:25]>CN(C)C=O>[Br:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][C:10]1[CH:9]=[CH:8][CH:7]=[C:3]2[C:4]([NH:5][C:1](=[O:11])[C:2]=12)=[O:6]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 199334951,8-DibromododecaneHCID 24194345Phthalimide potassium salt

Product 1

HCID 1993351212-Bromododecylphthalimide

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

Potassium phthalimide (1 g; 5.4 mmoles) was added to a solution of 1,8-dibromododecane (5.31 g; 16.2 mmoles) in dimethylformamide (8 ml) and heated to 80° C. approx. under stirring. Reaction times and process as per Example 4.

Workup

  1. temperature
heated to 80° C. approx.
  • customReaction times and process as per Example 4
  • Sources & evidence

    ORD record
    ord-2b1425fe22a64dcf83200dc045951830
    Source dataset
    uspto-grants-1994_04
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US05302593

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes