HRID233283

反应详情

EQUATION

反应方程式

HRID 233283 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
10 °C

PROCEDURE

实验过程

To a mixture of 5-amino-2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]pyridine (9.1 g), an aqueous solution of HBr (47%, 14.2 ml) and acetone (150 ml) was added dropwise, at temperature not exceeding 10° C. a solution of sodium nitrite (NaNO2) (2.33 g) in water (10 ml). The mixture was stirred for 30 minutes at 10° C., to which was added acrylonitrile (CH2 =CHCN) (12.1 ml). To the mixture was added, while stirring vigorously, copper(I) oxide (Cu2O) (0.1 g). The reaction mixture was stirred for further one hour at temperature ranging from 30° to 35° C., followed by concentration under reduced pressure. The concentrate was poured into water, which was made alkaline with a conc. ammonia water, followed by extraction with ethyl acetate. The ethyl acetate layer was washed with water and dried (MgSO4), then the solvent was distilled off under reduced pressure. The residual oily product was subjected to a silica gel column chromatography. From the fractions eluted with ethyl acetate--hexane (1:1, v/v), was obtained 2-bromo-3-[2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]-5-pyridyl]propionitrile (6.11 g, 48%), which was recrystallized from ethyl acetate--hexane to give colorless crystals, m.p.93°-94° C.

WORKUP

后处理

  1. customexceeding 10° C.
  2. additionTo the mixture was added
  3. stirringwhile stirring vigorously
  4. stirringThe reaction mixture was stirred for further one hour at temperature
  5. customranging from 30° to 35° C.
  6. concentrationfollowed by concentration under reduced pressure
  7. additionThe concentrate was poured into water, which
  8. extractionfollowed by extraction with ethyl acetate
  9. washThe ethyl acetate layer was washed with water
  10. dry with materialdried (MgSO4)
  11. distillationthe solvent was distilled off under reduced pressure
  12. washFrom the fractions eluted with ethyl acetate--hexane (1:1