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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378305Generated: October 25, 2026

L-Aspartic Acid → Ethylene Aspartate Cysteate

https://huagongshe.com/reaction/1378305

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-Aspartic AcidHCID 5960—
Reactant1,2-DibromoethaneHCID 7839—
ReactantSodium CarbonateHCID 10340—
ReactantSodium HydroxideHCID 14798—
ReactantL-Cysteic acidHCID 72886—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductEthylene Aspartate CysteateHCID 86751243—

Reaction Conditions

Temperature84 °C

Reaction Steps

A 500 ml three necked round bottom flask equipped with a mechanical stirrer, thermometer and reflux condenser was charged with 7.08 g (0.0532 mol) L-aspartic acid, 9.96 g (0.0532 mol) L-cysteic acid and 133 ml water. Add 8.51 g (0.2128 mol) sodium hydroxide and 5.64 g (0.0532 mol) sodium carbonate with moderate stirring. The reaction mixture exotherms to about 40° C. After all has dissolved, add 80 ml ethanol and 12.5 g (0.0665 mol) ethylene dibromide. Heat the reaction mixture to reflux (84° C.) for 24 hours. Replace the reflux condenser with a short path distillation head and distill off the ethanol and excess ethylene dibromide. Place flask in a water bath heated at 70° C. and remove trace amounts of ethylene dibromide under high vacuum. The crude yield of the reaction mixture was 31.08 g. This mixture was determined to contain salt, L-aspartic acid disodium salt, L-cysteic acid disodium salt, Na4EDC, Na4EDDS and Na4EAC. The purity of this product was found to be about 50-70% sequestrant by C13 nuclear magnetic resonance analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05668098
Source datasetuspto-grants-1997_09
ORD IDord-120695f2601c4e7dbfabe272aa2cfbda
Source noteuspto-grants-1997_09