Acetonitrile → 1-Phenyl-2-(1H-1,2,4-triazol-1-yl)propan-1-one

HRID 2166354Notes

Reaction equation

HRID 2166354 reaction equation
Br[CH:2]([CH3:11])[C:3]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=[O:4].N1C=[CH:15][N:14]=[N:13]1.[C:17](#[N:19])C>>[N:14]1([CH:2]([CH3:11])[C:3]([C:5]2[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=2)=[O:4])[CH:15]=[N:19][CH:17]=[N:13]1

Participants

4

Reactant 3

HCID 6342Acetonitrile2×HCID 164522-BromopropiophenoneHCID 178418936HCID 178418936, compound

Product 1

HCID 132599821-Phenyl-2-(1H-1,2,4-triazol-1-yl)propan-1-oneYield 55%

Procedure

To a solution of 223 g (1 mol) of 2-bromopropiophenone in 300 ml of acetonitrile is added dropwise to a boiling mixture of 414 g (6 mols) of triazole and 1,200 ml of acetonitrile, and the mixture is heated at the boil for 8 hours. Thereafter, the mixture is evaporated down in vacuo, the residue is taken up in 750 ml of dichloromethane and 750 ml of water, and the organic phase is washed with several 500 ml portions of water and dried over anhydrous sodium sulphate. After the solvent has been distilled off, the remaining residue is distilled in vacuo. 111 g (55% of theory) of 2-(1,2,4-triazol-1-yl)-propiophenone of boiling point 133° C./0.15 mbar and of melting point 117° C. are obtained. ##STR21##

Workup

  1. temperaturethe mixture is heated at the boil for 8 hours
  2. customThereafter, the mixture is evaporated down in vacuo
  3. wash750 ml of water, and the organic phase is washed with several 500 ml portions of water
  4. dry with materialdried over anhydrous sodium sulphate
  5. distillationAfter the solvent has been distilled off
  6. distillationthe remaining residue is distilled in vacuo

Sources & evidence

ORD record
ord-17777ef263d142faaeb1af6a7600d4ae
Source dataset
uspto-grants-1990_07
Patent number
US04945101

Reaction notes

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