Ammonium Chloride → HCID 178420208, compound

HRID 1773890Notes

Reaction equation

HRID 1773890 reaction equation
C([N:20]1[CH:24]=[C:23]([CH:25]=O)[N:22]=[CH:21]1)(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.[C:27]1([Mg]Br)[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1.[NH4+].[Cl-]>C1COCC1>[CH2:25]([C:23]1[N:22]=[CH:21][NH:20][CH:24]=1)[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1

Participants

5

Procedure

To a solution of 1-trityl-imidazole-4-carboxaldehyde (5 g, 14.8 mmoles) in THF (40 mL) is added dropwise a solution of 1M phenylmagnesium bromide in THF (17.7 mL, 17.7 mmoles). The reaction mixture is stirred at room temperature for 3 h, then it is poured into a saturated solution of NH4Cl. The aqueous phase is extracted three times with CH2Cl2. The organic phase is dried over magnesium sulphate, filtered and the solvent is removed under reduced pressure. The residue is dissolved in concentrated HI solution (75 mL) and the reaction mixture is heated at reflux overnight. After cooling at room temperature, the reaction mixture is extracted three times with Et2O. The aqueous phase is basified by adding solid Na2CO3 to pH 7, solid NaHSO3 is added until the red colour disappeared and the aqueous phase is extracted three times with Et2O. The organic phase is dried over magnesium sulphate, filtered and the solvent is removed under reduced pressure to give 4-benzyl-1H-imidazole.

Workup

  1. extractionThe aqueous phase is extracted three times with CH2Cl2
  2. dry with materialThe organic phase is dried over magnesium sulphate
  3. filtrationfiltered
  4. customthe solvent is removed under reduced pressure
  5. dissolutionThe residue is dissolved in concentrated HI solution (75 mL)
  6. temperaturethe reaction mixture is heated
  7. temperatureat reflux overnight
  8. temperatureAfter cooling at room temperature
  9. extractionthe reaction mixture is extracted three times with Et2O
  10. additionby adding solid Na2CO3 to pH 7, solid NaHSO3
  11. additionis added until the red colour
  12. extractionthe aqueous phase is extracted three times with Et2O
  13. dry with materialThe organic phase is dried over magnesium sulphate
  14. filtrationfiltered
  15. customthe solvent is removed under reduced pressure

Sources & evidence

ORD record
ord-d087cc9d16154b6d96380dc6fb9b4657
Source dataset
uspto-grants-2016_02
Patent number
US09255101B2

Reaction notes

Loading…