3-Cyanophenol → 3-(2H-Tetrazol-5-yl)phenol
Reaktionsgleichung
[C:1]([C:3]1[CH:4]=[C:5]([OH:9])[CH:6]=[CH:7][CH:8]=1)#[N:2].[N-:10]=[N+:11]=[N-:12].[Na+].[Cl-].[NH4+]>CN(C)C=O>[N:2]1[NH:10][N:11]=[N:12][C:1]=1[C:3]1[CH:4]=[C:5]([OH:9])[CH:6]=[CH:7][CH:8]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 160 °C
Versuchsvorschrift
A mixture of 3-cyanophenol (4.14 g, 34.75 mmol) (Aldrich), sodium azide (2.49 g, 38.23 mmol) (Aldrich) and ammonium chloride (2.05 g, 38.23 mmol) in N,N-dimethylformamide (30 mL) were heated to 160° C. for 18 hours. The reaction mixture was concentrated. The residue was purified by C18 column eluting with acetonitrile-water to give 3-(2H-tetrazol-5-yl)-phenol. (Yield 0.9 g, 16%).
Aufarbeitung
- concentrationThe reaction mixture was concentrated
- customThe residue was purified by C18 column
- washeluting with acetonitrile-water
Quellen und Nachweise
- ORD-Eintrag
- ord-f19a0ca0dcbb41f98078a35c837fac3a
- Quelldatensatz
- uspto-grants-2011_04
- Patentnummer
- US07932390B2
Notizen zur Reaktion
Wird geladen…