Reaktion #1857544
ord-81819ec5bb3a40008e2b5919bcd1f621
Reaktionsgleichung
Sodium hydride
2-[2-chloro-4-(4-chlorophenoxy)phenyl]-1-(1,2,4-triazol-1-yl)propan-2-ol
benzylbromide
→
desired compound
Ausbeute 68.9%
1-[2-benzyloxy-2-[2-chloro-4-(4-chlorophenoxy)phenyl]propyl]-1,2,4-triazole
Ausbeute 68.9%
Edukte
Reagenzien
Keine
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1Temperaturat reflux
- 2Extraktionthe mixture was extracted with dichloro methane (3×)
- 3SonstigeThe combined organic phases were dried
- 4Filtrationfiltered through a silica plug
- 5Sonstigeevaporated
- 6SonstigeThe crude product was purified by column chromatography
Vorschrift
Sodium hydride (0.04 g) was added to a solution of 2-[2-chloro-4-(4-chlorophenoxy)phenyl]-1-(1,2,4-triazol-1-yl)propan-2-ol (0.5 g) in THF (15 mL). After 30 min benzylbromide (0.27 g) was added and the mixture was stirred for 18 h at reflux. Brine was added and the mixture was extracted with dichloro methane (3×). The combined organic phases were dried, filtered through a silica plug and evaporated. The crude product was purified by column chromatography to yield 0.43 g of the desired compound.