戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 580600作成日:2026年10月26日

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

https://huagongshe.com/reaction/580600

反応式

関与物質

役割名称HCID仕込み量
反応物Acetone CyanohydrinHCID 6406—
反応物Acetic AnhydrideHCID 7918—
反応物1,1'-Ethylenebis(3,3,5,5-tetramethylpiperazinone)HCID 116979—
反応物N,N'-(2-amino-2-methylpropyl)ethylenediamineHCID 10898752—
触媒Sulfuric AcidHCID 1118—
溶媒DichloromethaneHCID 6344—
生成物1,1'-Ethylenebis(4-acetyl-3,3,5,5-tetramethyl-2-piperazinone)HCID 20134274—

反応条件

温度130 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04753979
出典データセットuspto-grants-1988_06
ORD IDord-5f5b2198d01f437dbb080742b5a1763a
出典メモuspto-grants-1988_06