Reacción #214971

ord-2a1dec5a3e8548bdbbd041124337cfa3

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONThe solution treated with 10.6 g
  2. 2
    workup.ADDITIONtreated dropwise with 10.6 g
  3. 3
    OtroAfter 75 min. the reaction is partitioned between water and methylene chloride
  4. 4
    OtroThe aqueous layer is separated
  5. 5
    Extracciónextracted two times more with methylene chloride
  6. 6
    SecadoThe combined methylene chloride layer is dried over sodium sulfate
  7. 7
    Concentraciónconcentrated in vacuo

Procedimiento

A 13.55 g. (50 mM) trans-3-amino-4-hydroxycyclopentene toluenesulfonate is dissolved in 75 ml. of water. The solution treated with 10.6 g. (10.0 mM) of sodium carbonate, cooled in an ice bath, and treated dropwise with 10.6 g. (50 mM) of trichloroethylchloroformate while stirring vigorously. After 75 min. the reaction is partitioned between water and methylene chloride. The aqueous layer is separated and extracted two times more with methylene chloride. The combined methylene chloride layer is dried over sodium sulfate and concentrated in vacuo. Crystals of trans-3-amino-4-hydroxy-cyclopentene-N-trichloroethyl urethane are formed during the concentration. These are collected three times, each time rinsing the crystals with ether crop 1, 6.12 g. m.p. 105.5°-106°; crop 2, 4.36 g., m.p. 105-106; crop 3, 1.28 g., m.p. 104-105°.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04256898uspto-grants-1981_03