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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108658Generated: October 31, 2026

Hydrochloric Acid → HCID 21192220, compound

https://huagongshe.com/reaction/1108658

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantN-(2,3-Epoxypropyl)phthalimideHCID 21601—
Reactant1,4,7-Tris(carboxymethyl)-1,4,7,10-tetraazacyclododecaneHCID 107830—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 21192220HCID 21192220—

Reaction Conditions

Temperature50 °C

Reaction Steps

50 g (144.3 mmol) of 1,4,7-tris(carboxymethyl)-1,4,7,10-tetraazacyclododecane (D03A) is dissolved in 250 ml of water, and the pH is set at 13 with 5N sodium hydroxide solution. Then, a solution of 38.12 g (187.6 mmol) of N(2,3-epoxypropyl)phthalimide (Aldrich) in 100 ml of dioxane is added in drops within one hour, stirred for 24 hours at 50° C., and the pH is kept at 13 by adding 5N sodium hydroxide solution. The solution is set at pH 2 with 10% hydrochloric acid and evaporated to the dry state in a vacuum. The residue is dissolved in some water and purified on an ion-exchange column (Reillex®=poly-(4-vinyl)pyridine (it is eluted with water). The main fractions are concentrated by evaporation in a vacuum, and final purification of the residue is achieved by chromatography on RP-18 (LiChroPrep®/mobile solvent: gradient that consists of tetrahydrofuran/methanol/water). After the main fractions are concentrated by evaporation, 63.57 g (71% of theory) of an amorphous solid is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06068831
Source datasetuspto-grants-2000_05
ORD IDord-27ef0d95530449e5b3eed4d561157bcd
Source noteuspto-grants-2000_05