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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603974Generated: November 1, 2026

Carbamic acid, ethyl ester → L-Glutamic acid, N-((phenylmethoxy)carbonyl)-

https://huagongshe.com/reaction/1603974

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbamic acid, ethyl esterHCID 5641—
ReactantBenzyl chloroformateHCID 10387—
ReactantL-Glutamic AcidHCID 33032—
ProductL-Glutamic acid, N-((phenylmethoxy)carbonyl)-HCID 70866—

Reaction Steps

A number of different blocking agents can be used to block the amine group on the glutamic acid. These blocking agents include acyl-type protecting groups, urethan protecting groups, alkyl-type protecting groups, and arylidene-type protecting groups. Alternatively, rather than using blocking agents, the amine group can be protonated to block its functionality. Preferably, blocking of the glutamic acid is achieved by reacting it with carbobenzoxy chloride in an aqueous alkaline solution to form N-carbobenzoxy glutamic acid, which is commonly referred to as Z-glutamic acid. This reaction is inexpensive and provides about a 90% yield of Z-glutamic acid. Alternatively, Z-glutamic acid can be obtained from Aldrich Chemical Company, 1001 West Saint Paul Avenue, Milwaukee, Wis. 53233. Z-glutamic acid has the following structure: ##STR1##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990266
Source datasetuspto-grants-1999_11
ORD IDord-8be28f8582784ec4b281c707614df2b0
Source noteuspto-grants-1999_11