Sodium Sulfate → 4-(Pentafluorophenyl)-1,2,4-triazoline-3,5-dione

HRID 1979614

Reaktionsgleichung

Reaktionsgleichung von HRID 1979614
[F:1][C:2]1[C:7]([N:8]2[C:12](=[O:13])[NH:11][NH:10][C:9]2=[O:14])=[C:6]([F:15])[C:5]([F:16])=[C:4]([F:17])[C:3]=1[F:18].S([O-])([O-])(=O)=O.[Na+].[Na+]>C(OCC)(=O)C>[F:15][C:6]1[C:7]([N:8]2[C:9](=[O:14])[N:10]=[N:11][C:12]2=[O:13])=[C:2]([F:1])[C:3]([F:18])=[C:4]([F:17])[C:5]=1[F:16]

Komponenten

4

Versuchsvorschrift

A 50 ml, three-necked flask is fitted with a gas-dispersion tube, a drying tube and a stirrer. 4-(Pentafluorophenyl)-urazole, 0.5 g (1.8 mM) is dissolved in 25 ml of ethyl acetate. Anhydrous sodium sulfate, 3 g, is added to remove water present in NO2. The reaction mixture is cooled in an ice bath, and nitrogen dioxide added slowly for 20 minutes. The mixture is allowed to stir for 20 minutes. The Na2SO4 is removed by filtration and the ethyl acetate removed with the rotary evaporator to yield a red oil. The residual solvent is removed with a vacuum pump to yield a crystalline solid, 0.35 g, mp 88°-91° C. The product is further purified by sublimation, mp 94°-96° C.

Aufarbeitung

  1. customA 50 ml, three-necked flask is fitted with a gas-dispersion tube, a drying tube and a stirrer
  2. customto remove water
  3. temperatureThe reaction mixture is cooled in an ice bath
  4. additionnitrogen dioxide added slowly for 20 minutes
  5. customThe Na2SO4 is removed by filtration
  6. customthe ethyl acetate removed with the rotary evaporator
  7. customto yield a red oil
  8. customThe residual solvent is removed with a vacuum pump
  9. customto yield a crystalline solid, 0.35 g, mp 88°-91° C
  10. customThe product is further purified by sublimation, mp 94°-96° C.

Quellen und Nachweise

ORD-Eintrag
ord-7b7ffcbd9c824cfe94e22cbd7543e2b4
Quelldatensatz
uspto-grants-1984_11
Patentnummer
US04481356

Verknüpfte Notizen

Wird geladen…