Hydrogen Bromide → 4-(1,2,4-Triazol-1-yl)phenol
Reaktionsgleichung
C[O:2][C:3]1[CH:8]=[CH:7][C:6]([N:9]2[CH:13]=[N:12][CH:11]=[N:10]2)=[CH:5][CH:4]=1.Br>>[N:9]1([C:6]2[CH:5]=[CH:4][C:3]([OH:2])=[CH:8][CH:7]=2)[CH:13]=[N:12][CH:11]=[N:10]1Komponenten
3
Versuchsvorschrift
A mixture of 8 parts of 1-(4-methoxyphenyl)-1H-1,2,4-triazole and 150 parts of a hydrobromic acid solution 48% is stirred and refluxed overnight. The reaction mixture is evaporated and the residue is triturated in 2-propanone. The product is filtered off and crystallized from ethanol, yielding 5.5 parts (74%) of 4-(1H-1,2,4-triazol-1-yl)phenol; mp. 255.4° C.
Aufarbeitung
- temperaturerefluxed overnight
- customThe reaction mixture is evaporated
- customthe residue is triturated in 2-propanone
- filtrationThe product is filtered off
- customcrystallized from ethanol
Quellen und Nachweise
- ORD-Eintrag
- ord-3ff94ba1f03f4720948e3526d8b7d529
- Quelldatensatz
- uspto-grants-1980_11
- Patentnummer
- US04232034
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