Reacción #214971
ord-2a1dec5a3e8548bdbbd041124337cfa3
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1workup.ADDITIONThe solution treated with 10.6 g
- 2workup.ADDITIONtreated dropwise with 10.6 g
- 3OtroAfter 75 min. the reaction is partitioned between water and methylene chloride
- 4OtroThe aqueous layer is separated
- 5Extracciónextracted two times more with methylene chloride
- 6SecadoThe combined methylene chloride layer is dried over sodium sulfate
- 7Concentraciónconcentrated 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°.