Phosphorus oxychloride → 2-Chloro-5-phenyloxazole
Reaktionsgleichung
[C:1]1([C:7]2[O:11][C:10](=S)[NH:9][CH:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.P(Cl)(Cl)([Cl:15])=O>C(N(CC)CC)C>[Cl:15][C:10]1[O:11][C:7]([C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)=[CH:8][N:9]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
5-Phenyl-2(3H)-oxazolethione (Acta. Chem. Scand. 23 2879 (1969)) (19.6 g, 0.11 m) and phosphorous oxychloride (70 ml) were stirred with cooling during the cautious addition of triethylamine (12.4 g, 0.123 m). The mixture was then heated under reflux for 20 hours, excess reagents removed under reduced pressure and the residue distilled in vacuo to give the title product as a colourless oil which solidified on standing, b.p. 96°-8° C/0.6 mm, m.p. 34° C.
Aufarbeitung
- temperatureThe mixture was then heated
- temperatureunder reflux for 20 hours
- customexcess reagents removed under reduced pressure
- distillationthe residue distilled in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-ff4aa09c23e1459388d2253bd77629ad
- Quelldatensatz
- uspto-grants-1979_03
- Patentnummer
- US04143047
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