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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701104Generated: November 1, 2026

Ethylenediamine → HCID 20348257, compound

https://huagongshe.com/reaction/1701104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylenediamineHCID 3301—
Reactant2,6-Diethyl-2,3,6-trimethylpiperidin-4-oneHCID 22182213—
CatalystHCID 178503042HCID 178503042—
SolventMethanolHCID 887—
ProductHCID 20348257HCID 20348257—

Reaction Steps

197.3 g of 2,6-diethyl-2,3,6-trimethylpiperidine-4-one and 30.0 g of ethylenediamine are dissolved in one liter of methanol. 10 g of a platin-carbon catalyst (5% b.w. Pt) are added, and the solution is hydrogenated at 30°-35° C. and normal pressure. Hydrogenation is completed after 106 hours. The catalyst is filtered off, the solvent is evaporated in vacuo, and the oily residue is purified by molecular distillation at 150° C. and 0.005 mm Hg. N,N'-Bis-(2,6-diethyl-2,3,6-trimethyl-4-piperidyl)-ethylenediamine (compound no. 7) is obtained as a practically colourless oil. If, instead of 30.0 g of ethylenediamine an equivalent amount of 1,6-hexamethylenediamine is used and otherwise the procedure described above is followed, after molecular distillation at 180° C. and 0.002 mm Hg. N,N'-Bis-(2,6-diethyl-2,3,6-trimethyl-4-piperidyl)-hexamethylene-1,6-diamine (compound no. 8) is obtained in the form of a thick colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04191683
Source datasetuspto-grants-1980_03
ORD IDord-29982e95c6664487915f8a630bb1267e
Source noteuspto-grants-1980_03