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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetone Cyanohydrin | HCID 6406 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 1,1'-Ethylenebis(3,3,5,5-tetramethylpiperazinone) | HCID 116979 | — |
| Reactant | N,N'-(2-amino-2-methylpropyl)ethylenediamine | HCID 10898752 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1,1'-Ethylenebis(4-acetyl-3,3,5,5-tetramethyl-2-piperazinone) | HCID 20134274 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04753979 |
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| Source dataset | uspto-grants-1988_06 |
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| ORD ID | ord-5f5b2198d01f437dbb080742b5a1763a |
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| Source note | uspto-grants-1988_06 |
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