Process for the preparation of substituted cyanophenoxy-pyrimidinyloxy-phenyl acrylate derivatives

Abstract

The present invention provides a process for reacting between a phenol derivative and an aromatic substrate under phenolate forming conditions comprising the following steps: (a) reacting a phenol derivative with a base in a polar organic solvent to obtain a phenolate salt, wherein water is removed from the reaction mixture during the reaction, (b) adding the aromatic substrate to the reaction mixture obtained in step (a), (c) heating the reaction mixture of step (b) to a temperature in the range of 80° to 1300° C., preferably, 90° to 1000° C. for 2 to 7 hours to obtain a phenoxy substituted aromatic substrate, (d) removing the solvent from the mixture of step (c) and optionally further isolating and purifying the phenoxy substituted aromatic substrate. Optionally, the removal of water during step (a) is in conjunction with partial removal of the organic solvent.

1 . A process for reacting a phenol derivative and an aromatic substrate under phenolate forming conditions comprising the following steps:
 a) reacting a phenol derivative with a base in a polar organic solvent to obtain a phenolate salt, wherein water is removed from the reaction mixture during the reaction,   b) adding the aromatic substrate to the reaction mixture comprising the phenolate salt obtained in step (a),   c) heating the reaction mixture of step (b) to a temperature in the range of 80° to 130° C. for 2 to 7 hours to obtain a phenoxy substituted aromatic substrate,   d) removing the solvent from the mixture of step (c) comprising the phenoxy substituted aromatic substrate.   
     
     
         2 . A process according to  claim 1 , wherein the removal of water during step (a) is in conjunction with partial removal of the polar organic solvent. 
     
     
         3 . A process according to  claim 1 , wherein the mole ratio between said phenol derivative and base is 1:1 to 1:1.5. 
     
     
         4 . A process according to  claim 1 , wherein the time required for step (a) to obtain conversion to the phenolate salt is 30 to 120 minutes at a temperature between 60° C. to 80° C., while partially removing solvent with water from the reaction mixture by vacuum distillation. 
     
     
         5 . A process according to  claim 1 , wherein the cyanophenol derivative is phenol, a mono-substituted phenol or a poly-substituted phenol. 
     
     
         6 . A process according to  claim 1 , wherein said base is selected from the group consisting of a hydroxide, a carbonate base, and a combination thereof. 
     
     
         7 . A process according to  claim 1 , wherein the polar organic solvent is selected from the group consisting of dimethyl formamide (DMF), dimethyl acetamide (DMAA), dimethyl sulphoxide (DMSO), and a combination thereof, and further wherein the reagent/solvent ratio is 0.1 mole/150 ml to 0.1 mole/350 ml. 
     
     
         8 . A process according to  claim 1 , wherein said aromatic substrate is added in step (b) together with a polar organic solvent. 
     
     
         9 . A process according to  claim 1 , wherein the aromatic substrate is added in an amount such that the mole ratio between the phenol derivative and aromatic substrate is between 1:0.8 and 1:1. 
     
     
         10 . A process according to  claim 1 , wherein the aromatic substrate is selected from the group consisting of mono- and poly-substituted pyridine, pyrimidine and phenyl groups. 
     
     
         11 . A process according to  claim 1 , comprising heating the reaction mixture of step (b) to a temperature in the range of 80° to 130° C. for 2 to 7 hours to obtain the phenoxy substituted aromatic substrate. 
     
     
         12 . A process according to  claim 1  for the preparation of methyl (E)-2-{2-[6-(2-cyanophenoxy)pyrimidin-4-yloxy]phenyl}-3-methoxyacrylate (azoxystrobin) comprising the following steps:
 a) reacting 2-cyanophenol with an alkali metal hydroxide or carbonate, in a polar organic solvent, at a temperature between 60° C. to 80° C., for about 1 hour, while removing the water which is formed during the reaction via distillation with the solvent under reduced pressure, 
 b) adding (E)-methyl 2-[2-(6-chlorpyridimin-4-yloxy)phenyl]-3-methoxypropenoate of formula (I) to the reaction mixture obtained in step (a), 
 
       
         
           
           
               
               
           
         
         c) heating the reaction mixture of step (b) to a temperature in the range of 80° to 130° C., for 2 to 7 hours, to obtain azoxystrobin, 
         d) removing the solvent from the mixture of step (c) by distillation under reduced pressure to obtain a crude azoxystrobin, 
         e) extracting the crude azoxystrobin with a non-polar organic solvent and water to obtain an organic and aqueous phase, and 
         f) crystallizing the azoxystrobin from the organic phase by cooling the organic solvent, filtering the precipitated solid and rinsing the precipitated solid with an alcohol to obtain azoxystrobin with a purity of 98%-99%. 
       
     
     
         13 . A process according to  claim 12 , wherein said base is sodium hydroxide, potassium hydroxide, sodium carbonate or potassium carbonate. 
     
     
         14 . A process according to  claim 12 , wherein said polar organic solvent is selected from the group consisting of dimethyl formamide (DMF), dimethyl acetamide (DMAA), dimethyl sulphoxide (DMSO), and a combination thereof. 
     
     
         15 . A process according to  claim 12 , wherein removing the water which is formed during the reaction of step (a) is via distillation with the solvent under reduced pressure, wherein the mole ratio between the 2-cyanophenol and the base is between 1:1 and 1:1.5. 
     
     
         16 . A process according to  claim 12 , wherein said non-polar organic solvent of step (e) is selected from the group consisting of toluene, xylene, at least C 4  acetate esters, and a combination thereof. 
     
     
         17 . A process according to  claim 12 , further comprising:
 a) reacting the 2-cyanophenol with sodium hydroxide in DMAA, DMSO, or a combination thereof, at a temperature between 60° C. to 80° C. for about 1 hour, while removing the water which is formed during the reaction via distillation with the solvent under a reduced pressure of about 20-30 mbar, wherein the mole ratio between the 2-cyanophenol and the sodium hydroxide is between 1:1 and 1:1.5;   b) adding (E)-methyl 2-[2-(6-chlorpyridimin-4-yloxy)phenyl]-3-methoxypropenoate of formula (I) as a solution in DMAA to the reaction mixture obtained in step (a),   
       
         
           
           
               
               
           
         
         c) heating the reaction mixture of step (b) to a temperature in the range of 90° C. to 100° C. for 4 to 6 hours to obtain azoxystrobin, 
         d) removing the solvent from the mixture of step (c) by distillation under reduced pressure to obtain a crude azoxystrobin, 
         e) extracting the crude azoxystrobin with butylacetate and water to obtain an organic and aqueous phase, and 
         f) crystallizing the azoxystrobin from the organic phase by cooling the organic solvent, filtering the precipitated solid and rinsing the precipitated solid with methanol to obtain azoxystrobin with a purity of 98%-99%. 
       
     
     
         18 . The process according to  claim 5 , wherein the phenol derivative is 2-cyanophenol or 4-cyanophenol. 
     
     
         19 . The process according to  claim 6 , wherein the base is selected from the group consisting of including metal hydroxides, alkali metal hydroxides, metal carbonates, alkali metal carbonates, and mixtures thereof. 
     
     
         20 . The process according to  claim 10 , wherein the aromatic substrate is a chloro-pyrimidine derivative.