Imidazole → 2-Hydroxy-4-imidazol-1-ylmethyl-benzonitrile
Reaktionsgleichung
Br[CH2:2][C:3]1[CH:10]=[CH:9][C:6]([C:7]#[N:8])=[C:5]([OH:11])[CH:4]=1.[NH:12]1[CH:16]=[CH:15][N:14]=[CH:13]1>CN(C=O)C>[OH:11][C:5]1[CH:4]=[C:3]([CH2:2][N:12]2[CH:16]=[CH:15][N:14]=[CH:13]2)[CH:10]=[CH:9][C:6]=1[C:7]#[N:8]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
4-Bromomethyl-2-hydroxy-benzonitrile (0.22 g, 1.05 mmol) and imidazole (0.36 g, 5.23 mmol) were dissolved in DMF (10 mL) with stirring at ambient temperature. After stirring for 18 h the reaction mixture was concentrated in vacuo and purified by silica gel chromatography eluting with 2% CH3OH/CH2Cl2 to 5% CH3OH/CH2Cl2 to give the title compound.
Aufarbeitung
- stirringAfter stirring for 18 h the reaction mixture
- concentrationwas concentrated in vacuo
- custompurified by silica gel chromatography
- washeluting with 2% CH3OH/CH2Cl2 to 5% CH3OH/CH2Cl2
Quellen und Nachweise
- ORD-Eintrag
- ord-fd218a04b3084973923057e2d5ebd771
- Quelldatensatz
- uspto-grants-2001_10
- Patentnummer
- US06297239B1
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