Reacción #5920

ord-d89b6b0a42ba47e2b52fd965ff8e6b9b

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONis added dropwise
  2. 2
    Lavadothe organic layer is washed
  3. 3
    Otrodried
  4. 4
    workup.DISTILLATIONAfter the solvent is distilled off
  5. 5
    Lavadothe resulting crystals are washed with n-hexane

Procedimiento

To a mixture of 2-(4-chlorophenyl)-3,4-dihydro-2H-1,4-benzothiazine (9.62 g), sodium hydrogen carbonate (6.0 g), methylene chloride (100 ml) and water (50 ml) is added dropwise with stirring a solution of acryloyl chloride (5.0 g) in methylene chloride (20 ml) under ice cooling over a period of about 30 minutes. The mixture is stirred at room temperature for 3 hours, and the organic layer is washed and dried. After the solvent is distilled off, the resulting crystals are washed with n-hexane to give 2-(4-chlorophenyl)-4-acryloyl-3,4-dihyro-2H-1,4-benzothiazine (10.76 g, yield 93%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05246929uspto-grants-1993_09