Reacción #74710

Ecuación de reacción

phosphorous diphenyl ester

p-nitrophenol

Z-Gly

→

glycine p-nitrophenyl ester

Rendimiento 75.0%

Disolventes

pyridine

pyridine

pyridine

pyridine

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.ADDITIONA mixture of 2.93 g
2. 2
   Otrothe mixture was further reacted for 1 hour
3. 3
   workup.ADDITIONTo the reaction mixture were added 2.61 g
4. 4
   Temperaturaunder reflux for 1 hour
5. 5
   Otrowas removed by distillation under reduced pressure
6. 6
   Extracciónthe residue was extracted with 100 ml
7. 7
   LavadoThe ethyl acetate layer was washed with 2 N
8. 8
   SecadoHCl, a saturated aqueous NaHCO3 solution and water in this order and then dried over anhydroush Na2SO4
9. 9
   Otroethyl acetate was removed by distillation under reduced pressure
10. 10
    Otroto form a solid, which
11. 11
    Otrowas then recrystallized from ethanol

Procedimiento

A mixture of 2.93 g. (0.0125 mole) of phosphorous diphenyl ester and 3.37 g. (0.0125 mole) of mercuric chloride was refluxed for 1 hour in 20 ml. of pyridine. Thereafter, 1.74 g. (0.0125 mole) of p-nitrophenol and 10 ml. of pyridine were added, and the mixture was further reacted for 1 hour. To the reaction mixture were added 2.61 g. (0.0125 mole) of Z-Gly.OH having an amino group protected with Z and 10 ml. of pyridine, and the mixture was reacted under reflux for 1 hour. After completion of the reaction, pyridine was removed by distillation under reduced pressure, and the residue was extracted with 100 ml. of ethyl acetate. The ethyl acetate layer was washed with 2 N--HCl, a saturated aqueous NaHCO3 solution and water in this order and then dried over anhydroush Na2SO4, and thereafter ethyl acetate was removed by distillation under reduced pressure. The resulting residue was allowed to stand to form a solid, which was then recrystallized from ethanol to obtain N-benzyloxycarbony glycine p-nitrophenyl ester (hereinafter represented by ##STR9## in a yield of 75% (3.0 g.).

Fuente