Réaction #4387

ord-4a0ab28d099d4c989edf76e5c61389c1

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrethe organic layer was separated
  2. 2
    Extractionthe aqueous layer was extracted with methylene chloride
  3. 3
    LavageThe combined extracts were washed with saturated sodium chloride aqueous solution
  4. 4
    Séchagedried over magnesium sulfate
  5. 5
    Autreevaporated in vacuo
  6. 6
    AutreThe 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).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US04725601uspto-grants-1988_02