反応 #65867

ord-61b678b9b6184ef6bc35ea82c07962dd

反応方程式

CCOC=C(C#N)C(=O)OC
ethoxymethylenecyanoacetic acid methyl ester
Cc1ccccc1
toluene
Cc1ccccc1
toluene
FC1(F)Oc2ccccc2O1
2,2-difluoro-1,3-benzodioxole
[Li][CH2]CCC
n-butyllithium
CN(C)CCN(C)C
TMEDA
CCOC(=O)/C(C#N)=C/c1cccc2c1OC(F)(F)O2
title compound
CCOC(=O)/C(C#N)=C/c1cccc2c1OC(F)(F)O2
(E)-2-cyano-3-(2,2-difluoro-1,3-benzodioxol-4-yl)-2-propenoic acid ethyl ester

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

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

実験手順

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.

出典

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