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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1283232Erstellt: 25. Oktober 2026

4-Nitrophenol → N-((Phenylmethoxy)carbonyl)glycine 4-nitrophenyl ester

https://huagongshe.com/reaction/1283232

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-NitrophenolHCID 980—
EduktBenzyloxycarbonylglycineHCID 14349—
EduktPhosphorous diphenyl esterHCID 426896—
LösungsmittelPyridineHCID 1049—
ProduktN-((Phenylmethoxy)carbonyl)glycine 4-nitrophenyl esterHCID 1561675%

Reaktionsschritte

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 2N--HCl, a saturated aqueous NaHCO3 solution and water in this order and then dried over anhydrous 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-benzyloxycarbonyl glycine p-nitrophenyl ester (hereinafter represented by ##SPC6##

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS03974219
Quelldatensatzuspto-grants-1976_08
ORD IDord-7f0fff29f3874cfb8a398bcae10b0ec3
Quellennotizuspto-grants-1976_08