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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354713Generated: October 27, 2026

Triethylamine → alpha,epsilon-dicarbobenzoxy-L-lysyl-L-phenylalanine benzyl ester

https://huagongshe.com/reaction/354713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantIsobutyl chloroformateHCID 62365—
Reactantp-ToluenesulfonateHCID 85570—
ReactantBenzyl 3-phenyl-L-alaninateHCID 736312—
Reactantalpha,epsilon-dicarbobenzoxy-L-lysineHCID 22822836—
SolventTolueneHCID 1140—
SolventChloroformHCID 6212—
Productalpha,epsilon-dicarbobenzoxy-L-lysyl-L-phenylalanine benzyl esterHCID 22822837—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of α,ε-dicarbobenzoxy-L-lysine (4) (96 mmol, 39.69 g), toluene (310 ml) and triethylamine (96 mmol, 9.70 g) at 0° C., was added, over a period of 15 minutes, iso-butyl chloroformate (109 mmol, 14.88 g), maintaining the temperature between -5° and 0° C. The resulting jelly-like reaction mixture was stirred for 30 minutes at 0° C. and then a slurry of L-phenylalanine benzyl ester, p-toluene sulphonate (1) (96 mmol, 40.99 g) in chloroform (470 ml) and triethylamine (96 mmol, 9.70 g) was added quickly in one portion and the clear solution was allowed to stir at ambient temperature overnight.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04376766
Source datasetuspto-grants-1983_03
ORD IDord-ac60421b493c45569276741815aa824e
Source noteuspto-grants-1983_03