関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetone Cyanohydrin | HCID 6406 | — |
| 反応物 | Acetic Anhydride | HCID 7918 | — |
| 反応物 | 1,1'-Ethylenebis(3,3,5,5-tetramethylpiperazinone) | HCID 116979 | — |
| 反応物 | N,N'-(2-amino-2-methylpropyl)ethylenediamine | HCID 10898752 | — |
| 触媒 | Sulfuric Acid | HCID 1118 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 1,1'-Ethylenebis(4-acetyl-3,3,5,5-tetramethyl-2-piperazinone) | HCID 20134274 | — |
反応手順
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.).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04753979 |
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| 出典データセット | uspto-grants-1988_06 |
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| ORD ID | ord-5f5b2198d01f437dbb080742b5a1763a |
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| 出典メモ | uspto-grants-1988_06 |
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