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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1596752Generated: November 3, 2026

Hydrochloric Acid → cis-1,3-Dibenzyl-2-imidazolidone-4,5-dicarboxylic acid

https://huagongshe.com/reaction/1596752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
ReactantPhenyl chloroformateHCID 15891—
ReactantD-Aspartic acid, N-(phenylmethyl)-3-((phenylmethyl)amino)-, (3S)-rel-HCID 108349—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Productcis-1,3-Dibenzyl-2-imidazolidone-4,5-dicarboxylic acidHCID 984151276%

Reaction Conditions

Temperature30 °C

Reaction Steps

220 g (0.67 mol) of meso-2,3-bis(benzylamino)succinic acid were placed under a nitrogen atmosphere in a 2 l flask fitted with two dropping funnels, a pH electrode, and a stirrer. The meso-2,3-bis(benzylamino)succinic acid was then suspended, while stirring, in 800 ml of tetrahydrofuran and 400 ml of deionized water and brought into solution by the addition of 108 ml of a 50% potassium hydroxide solution. 200 ml of 2.4 mole q. phenyl chloroformate were added dropwise to the solution within 3.5 hours. The pH was maintained between 9 and 11 during the addition of phenyl chloroformate by the successive addition of a 50% potassium hydroxide solution, and the internal temperature was maintained between 30° C. and 35° C. After the addition was completed, the mixture was stirred at about 30° C. for 2 hours and the pH was adjusted to about 7-8 with concentrated hydrochloric acid. The aqueous solution was then extracted twice with toluene and 500 ml of tetrahydrofuran were added to the combined aqueous phases. The mixture was adjusted to a pH of 1.0 with 37% hydrochloric acid and the aqueous phase was separated off. 400 ml of toluene were added to the tetrahydrofuran phase and the tetrahydrofuran was distilled off under reduced pressure. The remaining water was removed azeotropically with toluene. The residual brownish, oily solution was seeded and the crystalline solid was filtered off and washed twice with toluene. After drying to constant weight under reduced pressure, there were obtained 181.5 g (76% yield) of 2-oxo-1,3-dibenzyl-cis-4,5-imidazolidinedicarboxylic acid, with a melting point of 172.8° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06291681B1
Source datasetuspto-grants-2001_09
ORD IDord-24af591d1f3c438089bcca97b9f5972a
Source noteuspto-grants-2001_09