2,6-Diisopropylphenyl isocyanate → HCID 21957890, compound

HRID 2213623Notes

Reaction equation

HRID 2213623 reaction equation
[CH2:1]([NH:8][C:9]1[CH:14]=[CH:13][C:12]([CH2:15][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]([CH2:15][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]=1

Participants

3

Reactant 2

HCID 922592,6-Diisopropylphenyl isocyanateHCID 21957880HCID 21957880, compound

Product 1

HCID 21957890HCID 21957890, compound

Procedure

By the reaction and treatment in the same manner as in Example 2 using benzyl(4-octylphenyl)amine and 2,6-diisopropylphenyl isocyanate as starting materials, N-benzyl-N′-(2,6-diisopropylphenyl)-N-(4-octylphenyl)urea is obtained.

Sources & evidence

ORD record
ord-15a96afe658d455fa4437c524a092c59
Source dataset
uspto-grants-2006_09
Patent number
US07105567B2

Reaction notes

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