反应 #1096

ord-5d39e4809233431997c0a9624f5079c5

反应方程式

COc1c(Cl)ccnc1C
4-chloro-3-methoxy-2-methylpyridine
Oc1ccccc1
phenol
NOCc1ccccc1
O-benzylhydroxylamine
[Na+].[OH-]
NaOH
COc1c(NOCc2ccccc2)ccnc1C
4-(O-Benzylhydroxylamino)-3-methoxy-2-methylpyridine

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度After cooling
  2. 2
    萃取The aqueous phase is extracted a second time with CH2Cl2
  3. 3
    浓缩After concentrating the combined CH2Cl2 phases, excess O-benzylhydroxylamine
  4. 4
    workup.DISTILLATIONis distilled off in vacuo at 0.6 mm
  5. 5
    其他The residue crystallizes
  6. 6
    过滤After filtering off with suction
  7. 7
    洗涤washing with hexane 21.6 g=88.4% of product
  8. 8
    其他The product is recrystallized from ethyl acetate

实验过程

16 g of 4-chloro-3-methoxy-2-methylpyridine, 63 g of phenol and 40 g of O-benzylhydroxylamine are stirred at 120° C. under nitrogen for 4 hours. After cooling, the mixture is shaken with 500 ml of 2N NaOH and CH2Cl2. The aqueous phase is extracted a second time with CH2Cl2. After concentrating the combined CH2Cl2 phases, excess O-benzylhydroxylamine is distilled off in vacuo at 0.6 mm. The residue crystallizes on stirring with hexane. After filtering off with suction and washing with hexane 21.6 g=88.4% of product remain. The product is recrystallized from ethyl acetate. M.p.: 130° C.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05723450uspto-grants-1998_03