2,6-Diisopropylphenyl isocyanate → N-benzyl-N'-(2,6-diisopropylphenyl)-N-(4-heptyloxyphenyl)urea
Reaktionsgleichung
[CH2:1]([NH:8][C:9]1[CH:14]=[CH:13][C:12]([O:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22])=[CH:11][CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH:23]([C:26]1[CH:31]=[CH:30][CH:29]=[C:28]([CH:32]([CH3:34])[CH3:33])[C:27]=1[N:35]=[C:36]=[O:37])([CH3:25])[CH3:24]>>[CH2:1]([N:8]([C:9]1[CH:10]=[CH:11][C:12]([O:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH3:22])=[CH:13][CH:14]=1)[C:36]([NH:35][C:27]1[C:26]([CH:23]([CH3:24])[CH3:25])=[CH:31][CH:30]=[CH:29][C:28]=1[CH:32]([CH3:34])[CH3:33])=[O:37])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Komponenten
3
Versuchsvorschrift
By the reaction and treatment in the same manner as in Example 2 using benzyl(4-heptyloxyphenyl)amine (2.1 g) and 2,6-diisopropylphenyl isocyanate (1.61 g) as starting materials, N-benzyl-N′-(2,6-diisopropylphenyl)-N-(4-heptyloxyphenyl)urea (1.4 g) was obtained.
Quellen und Nachweise
- ORD-Eintrag
- ord-ec62e00908ef40f5966cb24936f0b8df
- Quelldatensatz
- uspto-grants-2006_09
- DOI