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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46432Generated: October 26, 2026

4-Nitrophenol → 4-Nitrophenyl glycinate

https://huagongshe.com/reaction/46432

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrophenolHCID 980—
ReactantBenzyloxycarbonylglycineHCID 14349—
ReactantPhosphorous diphenyl esterHCID 426896—
SolventPyridineHCID 1049—
Product4-Nitrophenyl glycinateHCID 15222475%

Reaction Steps

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.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04173563
Source datasetuspto-grants-1979_11
ORD IDord-5ad6475a7d1c436b9cd65875c1aa620e
Source noteuspto-grants-1979_11