反应 #65867

ord-61b678b9b6184ef6bc35ea82c07962dd

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他at from -15° to -10° C.
  2. 2
    其他the phases are separated
  3. 3
    浓缩the organic phase is concentrated by evaporation in a vacuum rotary evaporator

实验过程

53.3 g (337 mmol) of 2,2-difluoro-1,3-benzodioxole in 46 ml of toluene are metalated according to Example 2d), at from -15° to -10° C., with 137.8 g (409 mmol) of n-butyllithium solution (19.0% in toluene) in the presence of 39.3 g (339 mmol) of TMEDA. 69.1 g (409 mmol) of ethoxymethylenecyanoacetic acid methyl ester in 150 ml of toluene are metered in at from -15° to -10° C. over a period of 21/2 hours. The reaction mixture is added at +10° C. to 450 ml of water, the phases are separated and the organic phase is concentrated by evaporation in a vacuum rotary evaporator to yield the title compound.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05420301uspto-grants-1995_05