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Pyridine → 5-Chloro-3-phenyl-1,2,4-oxadiazole

HRID 1195798
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Reaktionsgleichung

Reaktionsgleichung von HRID 1195798
P(Cl)(Cl)([Cl:3])=O.[C:6]1([C:12]2[N:16]=[C:15](O)[O:14][N:13]=2)[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.N1C=CC=CC=1>>[C:6]1([C:12]2[N:16]=[C:15]([Cl:3])[O:14][N:13]=2)[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 1049PyridineHCID 24813Phosphorus oxychlorideHCID 178517464HCID 178517464, Verbindung

Produkt 1

HCID 127284435-Chloro-3-phenyl-1,2,4-oxadiazole

Versuchsvorschrift

To 53 g of phosphorus oxychloride were added 12.6 g (18 mmol) of 3-phenyl-1,2,4-oxadiazol-5-ol, followed by the further addition of 2.8 g (35 mmol of pyridine. The resultant mixture was heated under stirring for 8 hours. The reaction mixture was allowed to cool down to room temperature and then transferred into 500 ml of ice water. The resultant liquid mixture was extracted with ether. The extract was washed successively with water, a 5% aqueous solution of sodium hydroxide and water. The organic layer was dried and the solvent was distilled off. When the residue was left over under cooling, the title compound was obtained as pale brown crystals.

Aufarbeitung

  1. extractionThe resultant liquid mixture was extracted with ether
  2. washThe extract was washed successively with water
  3. customThe organic layer was dried
  4. distillationthe solvent was distilled off
  5. waitWhen the residue was left over
  6. temperatureunder cooling

Quellen und Nachweise

ORD-Eintrag
ord-4370dca4fe0d4759bff0dd6d450dc528
Quelldatensatz
uspto-grants-1992_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05112841

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