反应 #4387

ord-4a0ab28d099d4c989edf76e5c61389c1

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他the organic layer was separated
  2. 2
    萃取the aqueous layer was extracted with methylene chloride
  3. 3
    洗涤The combined extracts were washed with saturated sodium chloride aqueous solution
  4. 4
    干燥dried over magnesium sulfate
  5. 5
    其他evaporated in vacuo
  6. 6
    其他The crystalline residue was recrystallized from ethyl acetate

实验过程

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).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US04725601uspto-grants-1988_02