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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1274414Generated: November 3, 2026

1,2-Dichloroethane → 1,4,7,10-Tetraazacyclododecane

https://huagongshe.com/reaction/1274414

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantWaterHCID 962—
ReactantTriethylenetetramineHCID 5565—
ReactantGlyoxalHCID 7860—
ReactantPotassium HydroxideHCID 14797—
ReactantHydrazine hydrate (1:1)HCID 24654—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
Product1,4,7,10-TetraazacyclododecaneHCID 64963—

Reaction Steps

50 g of triethylenetetramine (0.342 mol) is dissolved in 1 ml of methanol and mixed at room temperature with 39 ml of 40% glyoxal in water (0.342 mol). After 20 hours of stirring, the solvent is distilled off in a vacuum, and an orange-colored oil is obtained, which then is taken up in 400 ml of dimethylformamide and mixed with 81.2 ml (101.5 g=1.026 mol) of 1,2-dichloroethane. After 8 hours of stirring at 40° C., it is concentrated by evaporation in a vacuum, the residue is taken up in 400 ml of ethanol and acidified to pH=3-4 with 37% aqueous hydrochloric acid. 166 ml (171 g=3.42 mol) of hydrazine hydrate is added to this reaction solution at room temperature, and it is heated under reflux for 30 hours. The reaction solution is set at pH=13 with solid potassium hydroxide. The reaction solution is subsequently concentrated by evaporation in a vacuum, taken up once more in 100 ml of ethanol, and the solvent is removed again in a vacuum. The residue is mixed with 25 g of activated carbon and 150 ml of formaldehyde diethylacetal, and it is heated under reflux for some time before the hot solution is filtered through a membrane. After the solution is cooled, the product is isolated by filtration.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06156890
Source datasetuspto-grants-2000_12
ORD IDord-2832f8b2e1de4f21a336af49485cf785
Source noteuspto-grants-2000_12