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HRID 580600Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/580600

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetone CyanohydrinHCID 6406—
EduktAcetic AnhydrideHCID 7918—
Edukt1,1'-Ethylenebis(3,3,5,5-tetramethylpiperazinone)HCID 116979—
EduktN,N'-(2-amino-2-methylpropyl)ethylenediamineHCID 10898752—
KatalysatorSulfuric AcidHCID 1118—
LösungsmittelDichloromethaneHCID 6344—
Produkt1,1'-Ethylenebis(4-acetyl-3,3,5,5-tetramethyl-2-piperazinone)HCID 20134274—

Reaktionsbedingungen

Temperatur130 °C

Reaktionsschritte

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.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04753979
Quelldatensatzuspto-grants-1988_06
ORD IDord-5f5b2198d01f437dbb080742b5a1763a
Quellennotizuspto-grants-1988_06