Hydrogen Bromide → HCID 70394003, compound

HRID 1383115Notes

Reaction equation

HRID 1383115 reaction equation
C(=O)([O-])O.[CH3:5][N:6]([CH3:34])[C:7]1[CH:33]=[CH:32][C:10]([CH:11]=[N:12][N+:13]2[CH:17]=[CH:16][N:15]([N:18]=[CH:19][C:20]3[CH:25]=[CH:24][C:23]([N:26]([CH3:28])[CH3:27])=[CH:22][CH:21]=3)[C:14]=2[CH:29]([CH3:31])[CH3:30])=[CH:9][CH:8]=1.[BrH:35]>O>[Br-:35].[CH3:28][N:26]([CH3:27])[C:23]1[CH:22]=[CH:21][C:20]([CH:19]=[N:18][N+:15]2[CH:16]=[CH:17][N:13]([N:12]=[CH:11][C:10]3[CH:32]=[CH:33][C:7]([N:6]([CH3:5])[CH3:34])=[CH:8][CH:9]=3)[C:14]=2[CH:29]([CH3:31])[CH3:30])=[CH:25][CH:24]=1

Participants

4

Reactant 2

HCID 260Hydrogen BromideHCID 70393745HCID 70393745, compound

Product 1

HCID 70394003HCID 70394003, compound

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

100 mg of 1,3-bis[[p-(dimethylamino)benzylidene]amino]-2-isopropylimidazolium hydrogen carbonate are suspended in 3 ml of water and 2 ml of 10 percent hydrogen bromide solution are added thereto. After 15 minutes the product is filtered, washed with water and recrystallized from ethanol. There is obtained 1,3-bis[[p-(dimethylamino)benzylidene]amino]-2-isopropylimidazolium bromide of melting point 241° (dec.).

Workup

  1. filtrationAfter 15 minutes the product is filtered
  2. washwashed with water
  3. customrecrystallized from ethanol

Sources & evidence

ORD record
ord-a66bbd63379a4659a581bbb003e21c8f
Source dataset
uspto-grants-1989_02
Patent number
US04808727

Reaction notes

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