Imidazole → HCID 131725032, compound
Reaction equation
[NH:1]1[CH:5]=[CH:4][N:3]=[CH:2]1.[B:6]([OH:9])([OH:8])[OH:7]>O>[B:6]([O-:9])([O-:8])[O-:7].[B:6]([O-:9])([O-:8])[O-:7].[B:6]([O-:9])([O-:8])[O-:7].[B:6]([O-:9])([O-:8])[O-:7].[B:6]([O-:9])([O-:8])[O-:7].[B:6]([O-:9])([O-:8])[O-:7].[B:6]([O-:9])([O-:8])[O-:7].[B:6]([O-:9])([O-:8])[O-:7].[B:6]([O-:9])([O-:8])[O-:7].[NH+:1]1[CH:5]=[CH:4][NH:3][CH:2]=1.[NH+:1]1[CH:5]=[CH:4][NH:3][CH:2]=1.[NH+:1]1[CH:5]=[CH:4][NH:3][CH:2]=1.[NH+:1]1[CH:5]=[CH:4][NH:3][CH:2]=1.[NH+:1]1[CH:5]=[CH:4][NH:3][CH:2]=1.[NH+:1]1[CH:5]=[CH:4][NH:3][CH:2]=1.[NH+:1]1[CH:5]=[CH:4][NH:3][CH:2]=1.[NH+:1]1[CH:5]=[CH:4][NH:3][CH:2]=1.[NH+:1]1[CH:5]=[CH:4][NH:3][CH:2]=1.[NH+:1]1[CH:5]=[CH:4][NH:3][CH:2]=1.[NH+:1]1[CH:5]=[CH:4][NH:3][CH:2]=1.[NH+:1]1[CH:5]=[CH:4][NH:3][CH:2]=1.[NH+:1]1[CH:5]=[CH:4][NH:3][CH:2]=1.[NH+:1]1[CH:5]=[CH:4][NH:3][CH:2]=1.[NH+:1]1[CH:5]=[CH:4][NH:3][CH:2]=1.[NH+:1]1[CH:5]=[CH:4][NH:3][CH:2]=1.[NH+:1]1[CH:5]=[CH:4][NH:3][CH:2]=1.[NH+:1]1[CH:5]=[CH:4][NH:3][CH:2]=1.[NH+:1]1[CH:5]=[CH:4][NH:3][CH:2]=1.[NH+:1]1[CH:5]=[CH:4][NH:3][CH:2]=1.[NH+:1]1[CH:5]=[CH:4][NH:3][CH:2]=1.[NH+:1]1[CH:5]=[CH:4][NH:3][CH:2]=1.[NH+:1]1[CH:5]=[CH:4][NH:3][CH:2]=1.[NH+:1]1[CH:5]=[CH:4][NH:3][CH:2]=1.[NH+:1]1[CH:5]=[CH:4][NH:3][CH:2]=1.[NH+:1]1[CH:5]=[CH:4][NH:3][CH:2]=1.[NH+:1]1[CH:5]=[CH:4][NH:3][CH:2]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 45 °C
Procedure
A flask fitted with a reflux condenser, magnetic stirrer, and temperature controller was charged with 225 mL deionized water and 70.0 g (1.0 moles) imidazole (C3H4N2). The resulting solution was heated to about 45° C. and 185.5 (3.0 moles) boric acid was added with stirring. The mixture was then heated to 90° C. and maintained with stirring for 1 h, cooled to 45° C., filtered, and washed with water. The resulting white powder was washed with about 100 mL deionized water and dried at 105° C. It was identified as imidazolium nonaborate by x-ray diffraction and titration analysis. Elemental analyses for the product are shown in Table 5, along with the theoretical analyses for imidazolium nonaborate, [C3H5N2]2O.3B2O3.2H2O.
Workup
- customA flask fitted with a reflux condenser, magnetic stirrer
- additiontemperature controller was charged with 225 mL
- temperatureThe mixture was then heated to 90° C.
- temperaturemaintained
- stirringwith stirring for 1 h
- temperaturecooled to 45° C.
- filtrationfiltered
- washwashed with water
- washThe resulting white powder was washed with about 100 mL
- customdried at 105° C
Sources & evidence
- ORD record
- ord-272b92e6f73f4d5ea90c8a5e48dad16b
- Source dataset
- uspto-grants-2005_07
- Patent number
- US06919036B2
Reaction notes
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