Reacción #63642

ord-3c8572f9eb4c498cba0e77d5e3eba59e

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Lavadowashed with a dilute solution of hydrochloric acid
  2. 2
    Lavadowash
  3. 3
    Lavadoa wash of dilute sodium hydroxide solution
  4. 4
    Lavadofinally by a wash of a saturated solution of sodium chloride
  5. 5
    SecadoThe reaction mixture is dried over anhydrous magnesium sulfate
  6. 6
    Otroevaporated to dryness

Procedimiento

A solution of 1.21 g of trans-3,4,4a,5,6,11b-hexahydro-2H-[1]benzoxepino[5,4-b]-1,4-oxazine hydrochloride, prepared according to the procedure of Example 2, and 1.65 ml of triethylamine in 25 ml of methylene chloride is treated dropwise with a solution of 0.70 ml of chloroacetyl chloride dissolved in 10 ml of methylene chloride. The reaction mixture is stirred overnight at room temperature, washed with a dilute solution of hydrochloric acid, followed by a water wash, a wash of dilute sodium hydroxide solution and finally by a wash of a saturated solution of sodium chloride. The reaction mixture is dried over anhydrous magnesium sulfate and evaporated to dryness to obtain 1.44 g of trans-N-chloroacetyl-3,4,4a,5,6,11b-hexahydro-2H-[1]-benzoxepino[5,4-b]-1,4-oxazine.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04766212uspto-grants-1988_08