Reacción #51666

ord-52c4651d64e1430795428fe882f2b19a

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroAfter 90 minutes the entire reaction mixture
  2. 2
    Lavadothe product was washed free of the acid
  3. 3
    Lavadoby eluting with 1:1 ethyl acetate

Procedimiento

The crude solid N-(2-chloro-6-methylsulfanylmethyl-phenyl)-2,2,2-trifluoro-acetamide from Step 2 was redissolved in methylene chloride (300 ml) and treated at 0° C. with meta-chloroperoxybenzoic acid (39.88 g, 0.177 mole) in portions with stirring. After 90 minutes the entire reaction mixture was poured onto a column of deactivated aluminum oxide (6% water) and the product was washed free of the acid by eluting with 1:1 ethyl acetate:hexane to afford 22.28 g of N-(2-Chloro-6-methanesulfonylmethyl-phenyl)-2,2,2-trifluoro-acetamide, a crystalline product (86%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06852726B2uspto-grants-2005_02