Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580600Generated: October 25, 2026

Acetone Cyanohydrin → 1,1'-Ethylenebis(4-acetyl-3,3,5,5-tetramethyl-2-piperazinone)

https://huagongshe.com/reaction/580600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetone CyanohydrinHCID 6406—
ReactantAcetic AnhydrideHCID 7918—
Reactant1,1'-Ethylenebis(3,3,5,5-tetramethylpiperazinone)HCID 116979—
ReactantN,N'-(2-amino-2-methylpropyl)ethylenediamineHCID 10898752—
CatalystSulfuric AcidHCID 1118—
SolventDichloromethaneHCID 6344—
Product1,1'-Ethylenebis(4-acetyl-3,3,5,5-tetramethyl-2-piperazinone)HCID 20134274—

Reaction Conditions

Temperature130 °C

Reaction Steps

31.5 grams (0.1 mole) of 1,1'-ethylenebis(3,3,5,5-tetramethyl-2-piperazinone), prepared according to Example 6, E of U.S. Pat. No. 4,190,571 from N,N'-(2-amino-2-methylpropyl)ethylenediamine and acetone cyanohydrin, is dissolved in 102 grams (1.0 mole) of acetic anhydride. After three drops of concentrated sulfuric acid are added to the solution, the mixture is heated for four hours at 130° C. and then cooled to room temperature. Methylene chloride (200 ml.) is added to extract the product into an organic layer which is then washed successively with water and with saturated sodium bicarbonate solution and is finally dried over anhydrous magnesium sulfate. The solvent is removed in vacuo and the residual product is recrystallized from toluene to give 30.4 grams of the above-named product as a white solid, melting at 180°-183° C. (sintering at 170° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04753979
Source datasetuspto-grants-1988_06
ORD IDord-5f5b2198d01f437dbb080742b5a1763a
Source noteuspto-grants-1988_06