Imidazole → HCID 131725032, compound

HRID 895961Notes

Reaction equation

HRID 895961 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]=1

Participants

4

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

  1. customA flask fitted with a reflux condenser, magnetic stirrer
  2. additiontemperature controller was charged with 225 mL
  3. temperatureThe mixture was then heated to 90° C.
  4. temperaturemaintained
  5. stirringwith stirring for 1 h
  6. temperaturecooled to 45° C.
  7. filtrationfiltered
  8. washwashed with water
  9. washThe resulting white powder was washed with about 100 mL
  10. 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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