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Hydrochloric Acid → 4-Methyl-2,3,5,6-tetrafluorobenzonitrile

HRID 1153713
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1153713
P(Cl)(Cl)(Cl)=O.[F:6][C:7]1[C:12]([F:13])=[C:11]([C:14]([NH2:16])=O)[C:10]([F:17])=[C:9]([F:18])[C:8]=1[CH3:19].Cl>C(Cl)Cl.N1C=CC=CC=1>[C:14]([C:11]1[C:10]([F:17])=[C:9]([F:18])[C:8]([CH3:19])=[C:7]([F:6])[C:12]=1[F:13])#[N:16]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 313Hydrochloric AcidHCID 24813Phosphorus oxychlorideHCID 204362822,3,5,6-Tetrafluoro-4-toluamide

Produkt 1

HCID 117887354-Methyl-2,3,5,6-tetrafluorobenzonitrile

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 1049PyridineLösungsmittelHCID 6344
Dichloromethane
Lösungsmittel

Versuchsvorschrift

A solution of phosphorus oxychloride (1.4 g) in methylene chloride (4 ml) was added slowly to a solution of 2,3,5,6-tetrafluoro-4-toluamide (1.0 g) in pyridine (8 ml) at -5° C. When the addition was complete the mixture was warmed to the ambient temperature over a period of 90 minutes, poured into a mixture of dilute hydrochloric acid and ice, and the resultant mixture was extracted with methylene chloride. After washing the extract with water (three times) and drying over anhydrous magnesium sulphate, the solvent was removed by evaporation under reduced pressure. The residual oil was purified by distillation under water pump pressure in a Kugelrohr apparatus to yield 4-cyano-2,3,5,6-tetrafluorotoluene, identified by infra red spectroscopy.

Aufarbeitung

  1. additionWhen the addition
  2. extractionthe resultant mixture was extracted with methylene chloride
  3. washAfter washing the
  4. extractionextract with water (three times)
  5. dry with materialdrying over anhydrous magnesium sulphate
  6. customthe solvent was removed by evaporation under reduced pressure
  7. distillationThe residual oil was purified by distillation under water

Quellen und Nachweise

ORD-Eintrag
ord-eccec0ae257c4863a193df954b6def43
Quelldatensatz
uspto-grants-1984_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04486355

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