Réaction #4387
ord-4a0ab28d099d4c989edf76e5c61389c1
Équation de réaction
Réactifs
Conditions de réaction
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1Autrethe organic layer was separated
- 2Extractionthe aqueous layer was extracted with methylene chloride
- 3LavageThe combined extracts were washed with saturated sodium chloride aqueous solution
- 4Séchagedried over magnesium sulfate
- 5Autreevaporated in vacuo
- 6AutreThe crystalline residue was recrystallized from ethyl acetate
Mode opératoire
To a mixture of 2-amino-3-hydroxypyridine (7 g) and Adogen 464 (Trademark: prepared by Aldrich Chemical Co.) (0.4 g) in 40% aqueous sodium hydroxide (32 ml) and methylene chloride (32 ml) was added 2-methylbenzyl chloride (8.42 ml) at ambient temperature. After being stirred for 24 hours, the organic layer was separated and the aqueous layer was extracted with methylene chloride. The combined extracts were washed with saturated sodium chloride aqueous solution, dried over magnesium sulfate, and evaporated in vacuo. The crystalline residue was recrystallized from ethyl acetate to give 2-amino-3-(2-methylbenzyloxy)pyridine (7.56 g).