Reacción #8925

ord-d52e816d05f1498dbac26bd0c69dc46e

Condiciones de reacción

Temperatura
-78°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroA 100 mL round bottom flask equipped with magnetic stir bar
  2. 2
    TemperaturaAfter 20 minutes the reaction was warmed to room temperature
  3. 3
    Concentraciónconcentrated in vacuo
  4. 4
    Otroto afford a white solid
  5. 5
    Filtraciónfiltered
  6. 6
    Otroto remove inorganic salts
  7. 7
    Concentraciónconcentrated in vacuo

Procedimiento

A 100 mL round bottom flask equipped with magnetic stir bar was charged with 1.22 g of benzyl 3-chlorosulfonyl-2(R)-methylpropionate in 15 mL CH2Cl2 and cooled to −78° C. To this solution was added to 10 mL of liquid ammonia at −78° C. After 20 minutes the reaction was warmed to room temperature, concentrated in vacuo to afford a white solid. The solid was slurried in ethyl acetate, filtered to remove inorganic salts and concentrated in vacuo to afford 1.08 g of benzyl 3-aminosulfonyl-2(R)-methylpropionate as a clear yellow oil. The crude product was used without further purification.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07091219B2uspto-grants-2006_08