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

HRID 483116Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 483116
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

Komponenten

4

Edukt 3

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

Produkt 1

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

Versuchsvorschrift

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##

Aufarbeitung

  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

Quellen und Nachweise

ORD-Eintrag
ord-4f62a252fa864e88abf63685df811bea
Quelldatensatz
uspto-grants-1986_03
Patentnummer
US04578396

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