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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174Generated: October 23, 2026

tert-Butyl acetate → N2-[(Phenylmethoxy)carbonyl]-L-lysine tert-Butyl Ester

https://huagongshe.com/en/reaction/1174

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl acetateHCID 10908—
ReactantSodium HydroxideHCID 14798—
ReactantPerchloric AcidHCID 24247—
ReactantN-alpha-Benzyloxycarbonyl-L-lysineHCID 75172—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductN2-[(Phenylmethoxy)carbonyl]-L-lysine tert-Butyl EsterHCID 11078219—

Reaction Steps

A mixture of 25 g of Nα-CBZ-L-lysine from Sigma, where CBZ is benzyloxycarbonyl, 250 mL of t-butyl acetate and 14 mL of 70% perchloric acid was vigorously mixed until all solids were dissolved. After stirring overnight, 375 mL of ethyl acetate was added followed by 250 mL of water. The pH of the aqueous layer was raised to 5.5 with 20% NaOH whereupon the organic phase was separated. The aqueous phase was extracted with the ethyl acetate solution and the pH again raised to 10.5 whereupon it was again extracted with 200 mL of fresh ethyl acetate. The organic extracts were combined, washed with saturated brine, dried over Na2SO4 and concentrated. The residue was dried overnight under high vacuum to yield 23.2 g of a colorless, viscous material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05723619
Source datasetuspto-grants-1998_03
ORD IDord-138236e224a34c72b9402d81270c32cc
Source noteuspto-grants-1998_03