Reaction #65866

ord-7d92c00c0e584bdda70e88162aee2abd

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Otherat from -15° to -10° C.
  2. 2
    Otherthe aqueous phase is separated off
  3. 3
    Concentrationthe organic phase is concentrated by evaporation in a vacuum rotary evaporator

Procedure

40.0 g (253 mmol) of 2,2-difluoro-1,3-benzodioxole in 29.5 g (254 mmol) of TMEDA and 35 ml of toluene are metallated analogously to Example 2c) at from -15° to -10° C. with 106.2 g (307 mmol) of n-butyllithium solution (18.5% in toluene). 52.1 g (308 mmol) of ethoxymethylenecyanoacetic acid ethyl ester in 115 ml of toluene are added to the reaction mixture at from -15° to -10° C. over a period of 2 hours. The resulting suspension is poured, after 20 minutes at +10° C., into 350 ml of water, the aqueous phase is separated off and the organic phase is concentrated by evaporation in a vacuum rotary evaporator to yield the desired product.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05420301uspto-grants-1995_05