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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362744Generated: October 25, 2026

Potassium Hydroxide → HCID 15017880, compound

https://huagongshe.com/reaction/362744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant1,4,7-Tris(carboxymethyl)-1,4,7,10-tetraazacyclododecaneHCID 107830—
ReactantHCID 15017879HCID 15017879—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 15017880HCID 15017880—

Reaction Conditions

Temperature40 °C

Reaction Steps

12.3 g (51.97 mmol) of 2,3-epoxy-1-[4-(5-hydroxypentyl)-phenoxy]-propane and 10 g (28.87 mmol) of 1,4,7-triscarboxymethyl-1,4,7,10-tetraazacyclododecane (=DO3A) are dissolved in a mixture of 50 ml of dioxane and 80 ml of water, and the pH is brought to pH 10 with 6N potassium hydroxide solution. It is stirred for 24 hours at 40° C. It is evaporated to dryness, the residue is taken up with 200 ml of water/50 ml of methanol and extracted twice with 100 ml of tert-butyl methyl ether. The aqueous solution is adjusted to pH 3 with 5N hydrochloric acid and evaporated to dryness. The residue is concentrated by evaporation in a vacuum and boiled out (extracted) with 200 ml of methanol/50 ml of methylene chloride. It is cooled in an ice bath and filtered off from precipitated potassium chloride. The filtrate is concentrated by evaporation in a vacuum, the residue is dissolved in 50 ml of water/20 ml of ethanol and then added to a column of poly-(4-vinylpyridine). The product is eluted with a solution of ethanol/water. After concentration by evaporation in a vacuum, 8.92 g (53% of theory) of the title compound is obtained as strongly hygroscopic, vitreous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05871709
Source datasetuspto-grants-1999_02
ORD IDord-4476f4d8e8f3459e9679a096b3d99a25
Source noteuspto-grants-1999_02