Reacción #51667

Ecuación de reacción

N-(2-Chloro-6-methanesulfonylmethyl-phenyl)-2,2,2-trifluoro-acetamide

sodium hydroxide

→

2-chloro-6-methanesulfonylmethyl-phenylamine

Rendimiento 90.0%

Condiciones de reacción

Tratamiento posterior

1. 1
   Temperaturaheated in an oil bath
2. 2
   workup.STIRRINGThe homogeneous solution was stirred at this temperature for 90 minutes
3. 3
   Temperaturato cool to room temperature
4. 4
   OtroThe flask was immersed in an ice bath
5. 5
   workup.ADDITIONthe suspension of the product
6. 6
   workup.STIRRINGwas stirred at this temperature until all was crystalline
7. 7
   FiltraciónFiltration
8. 8
   Lavadowashing well with water
9. 9
   Otrothorough drying

Procedimiento

The crystalline N-(2-Chloro-6-methanesulfonylmethyl-phenyl)-2,2,2-trifluoro-acetamide of Step 3 was taken up into 200 ml of 2N solution of sodium hydroxide and stirred and heated in an oil bath heated to 120° C. The homogeneous solution was stirred at this temperature for 90 minutes and slowly allowed to cool to room temperature. The flask was immersed in an ice bath and the suspension of the product was stirred at this temperature until all was crystalline. Filtration, washing well with water and thorough drying afforded 13.96 g of pure crystalline 2-chloro-6-methanesulfonylmethyl-phenylamine (90%).

Fuente