Réaction #502097
ord-168cdef8280448c485a0f1aa1909b388
Équation de réaction
sodium borohydride
5-[2-(4-chlorophenyl)imidazo[1,2-a]pyridin-6-yl]furan-2-carbaldehyde
→
compound
Rendement 37.3%
{5-[2-(4-Chlorophenyl)imidazo[1,2-a]pyridin-6-yl]furan-2-yl}methanol
Rendement 37.3%
Réactifs
Aucun
Solvants
Conditions de réaction
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1Autrethe solvent is then evaporated off under reduced pressure
- 2AutreThe organic phase is separated
- 3Séchagedried over sodium sulphate
- 4Concentrationconcentrated under reduced pressure
Mode opératoire
122 mg of sodium borohydride are added, in small portions, to 104 mg of 5-[2-(4-chlorophenyl)imidazo[1,2-a]pyridin-6-yl]furan-2-carbaldehyde dissolved in 20 ml of methanol. The mixture is subsequently stirred at ambient temperature for 2 hours, and the solvent is then evaporated off under reduced pressure. The residue is taken up between dichloromethane and water. The organic phase is separated, dried over sodium sulphate and concentrated under reduced pressure. 39 mg of compound are obtained.