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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197732Generated: October 31, 2026

Potassium Hydroxide → 10-[2-Hydroxy-3-(4-(5-hydroxypentyl)-phenoxy)-propyl]-1,4,7-tris(carboxymethyl)-1,4,7,10-tetraazacyclododecane

https://huagongshe.com/reaction/1197732

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant1,4,7-Tris(carboxymethyl)-1,4,7,10-tetraazacyclododecaneHCID 107830—
Reactant2,3-Epoxy-1-[4-(5-hydroxypentyl)-phenoxy]-propaneHCID 15017879—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product10-[2-Hydroxy-3-(4-(5-hydroxypentyl)-phenoxy)-propyl]-1,4,7-tris(carboxymethyl)-1,4,7,10-tetraazacyclododecaneHCID 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 numberUS05277895
Source datasetuspto-grants-1994_01
ORD IDord-ed3fe03574a44af99313f4afdfc4b7a9
Source noteuspto-grants-1994_01