Triethylenetetramine → HCID 19798169、化合物
反応式
[CH2:1]([CH:11]([C:17]([O-:19])=O)[C:12]([O:14]CC)=O)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10].[NH2:20][CH2:21][CH2:22][NH:23][CH2:24][CH2:25][NH:26][CH2:27][CH2:28][NH2:29]>C(O)C>[CH2:1]([CH:11]1[C:12](=[O:14])[NH:29][CH2:28][CH2:27][NH:26][CH2:25][CH2:24][NH:23][CH2:22][CH2:21][NH:20][C:17]1=[O:19])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10]参加物
4
実験手順
A one liter round bottomed flask was charged with 0.053 mol (15.9 g) of ethyl n-decylmalonate, 0.053 mol (7.738 g) triethylene tetramine, and 500 ml absolute ethanol. During refluxing for 42 days, 2 ml aloquotes were removed by hypodermic syringe on days 7, 15, 22, and 37 for NMR analysis to determine the completeness of the reaction. After termination of the reflux the ethanol was distilled away and the product recrystallized from cold acetonitrile to yield 10.89 g of a very light fluffy white precipitate representing approximately a 60.0% conversion to the titled compound.