Acetic Acid → HCID 70393775, compound
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.[C:35]([OH:38])(=[O:37])[CH3:36]>CO>[C:35]([O-:38])(=[O:37])[CH3:36].[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]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
1.3 g of 1,3-bis[[p-(dimethylamino)benzylidene]amino]-2-isopropylimidazolium hydrogen carbonate are dissolved in 10 ml of methanol and 2 ml of glacial acetic acid are added thereto. After stirring at room temperature for 16 hours, the solution is concentrated and the product is crystallized by the addition of ether. After two-fold recrystallization from methanol/ether, there is obtained 1,3-bis[[p-(dimethylamino)benzylidene]amino]2-isopropylimidazolium acetate of melting point 150°-151°.
Workup
- concentrationthe solution is concentrated
- customthe product is crystallized by the addition of ether
- customAfter two-fold recrystallization from methanol/ether
Sources & evidence
- ORD record
- ord-363b12bb9c40448296d30352a9586101
- Source dataset
- uspto-grants-1989_02
- Patent number
- US04808727
Reaction notes
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