Reacción #50050

ord-059ad3eb93334f9eaf7c76044c9fddb6

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONthe solution temperature below 10° C. (pH=11 after addition)
  2. 2
    LavadoThe remaining 2,2-dichloropropionylchloride was rinsed in with an additional 20 mL of methylene chloride
  3. 3
    Temperaturathe reaction mixture then warmed to at least 22° C.
  4. 4
    Otrothe reaction mixture were transferred to a 1 L flask with an additional 200 mL of water as a rinse
  5. 5
    OtroThe methylene chloride was removed by evaporation
  6. 6
    Filtraciónthe solid which forms was collected by filtration
  7. 7
    Lavadoa rinse

Procedimiento

To a dry 250 mL 3-necked flask were added L-proline (27 g., 0.235 moles, 1.0 eq.) and 100 mL of 6N sodium hydroxide. The solution (pH=14) was cooled to below 10° C. in an ice bath. A solution of dichloropropionylchloride (51.7 g., 0.32 moles, 1.37 eq.) in 40 mL of methylene chloride then was added over 60 minutes keeping the solution temperature below 10° C. (pH=11 after addition). The remaining 2,2-dichloropropionylchloride was rinsed in with an additional 20 mL of methylene chloride and the reaction mixture then warmed to at least 22° C. and stirred for 60 minutes, then the reaction mixture were transferred to a 1 L flask with an additional 200 mL of water as a rinse. The methylene chloride was removed by evaporation and the pH adjusted to 2. Upon cooling to 0° C. for 40 minutes, the solid which forms was collected by filtration using cold water as a rinse to yield N-(2,2-dichloropropionyl)proline which was dried under vacuum (0.1 Torr) for 15 hours to give 44.3 g. (78% yield) which can be further purified through recrystallization from ethyl acetate or ethyl acetate:hexane. m.p. 61°-62° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05424454uspto-grants-1995_06