Allylamine → N-[1-(t-Butylazo)cyclohexyl]-N'-allylthiourea
反応式
[C:1]([N:5]=[N:6][C:7]1([N:13]=[C:14]=[S:15])[CH2:12][CH2:11][CH2:10][CH2:9][CH2:8]1)([CH3:4])([CH3:3])[CH3:2].[CH2:16]([NH2:19])[CH:17]=[CH2:18]>CCCCC>[C:1]([N:5]=[N:6][C:7]1([NH:13][C:14]([NH:19][CH2:16][CH:17]=[CH2:18])=[S:15])[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12]1)([CH3:4])([CH3:2])[CH3:3]参加物
4
実験手順
To 9.6 grams (.0416 moles) of 1-t-butylazo-1-isothiocyanatocyclohexane cooled to 10° C. and stirred with a magnetic stirrer in a 50 ml erlenmeyer flask was added 2.37 grams (.0416 moles) of allylamine. The reaction mixture became viscous, was diluted with pentane and stirred for 24 hours at room temperature. The pentane was stripped from the reaction mixture to leave an orange liquid weighing 11.3 grams (94% crude yield). The infrared spectrum of the product had a strong band at 1525 cm-1 and a sharp NH band at 3300 cm-1 and the isothiocyante band at 2040 cm-1 was very weak indicating a trace of the starting material was still present.