2,6-Diisopropylphenyl isocyanate → HCID 10111262, compound

HRID 2213638Notes

Reaction equation

HRID 2213638 reaction equation
[CH2:1]([NH:5][C:6]1[CH:11]=[CH:10][C:9]([CH:12]([CH3:14])[CH3:13])=[CH:8][CH:7]=1)[CH2:2][CH2:3][CH3:4].[CH:15]([C:18]1[CH:23]=[CH:22][CH:21]=[C:20]([CH:24]([CH3:26])[CH3:25])[C:19]=1[N:27]=[C:28]=[O:29])([CH3:17])[CH3:16]>>[CH2:1]([N:5]([C:6]1[CH:7]=[CH:8][C:9]([CH:12]([CH3:13])[CH3:14])=[CH:10][CH:11]=1)[C:28]([NH:27][C:19]1[C:18]([CH:15]([CH3:16])[CH3:17])=[CH:23][CH:22]=[CH:21][C:20]=1[CH:24]([CH3:26])[CH3:25])=[O:29])[CH2:2][CH2:3][CH3:4]

Participants

3

Reactant 2

HCID 922592,6-Diisopropylphenyl isocyanateHCID 21957948HCID 21957948, compound

Product 1

HCID 10111262HCID 10111262, compoundYield 35%

Procedure

By the reaction and treatment in the same manner as in Example 2 using butyl(4-isopropylphenyl)amine (1.8 g) and 2,6-diisopropylphenyl isocyanate (2.7 g) as starting materials, N-butyl-N′-(2,6-diisopropylphenyl)-N-(4-isopropylphenyl)urea (1.3 g) was obtained.

Sources & evidence

ORD record
ord-b913f1252fac401a951e382b0d0bcde6
Source dataset
uspto-grants-2006_09
Patent number
US07105567B2

Reaction notes

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