1-Isocyanato-2-phenylbenzene → N-(2-hydroxy-4-trifluoromethylphenyl) N'-(2-phenylphenyl)urea

HRID 567992

Reaction equation

HRID 567992 reaction equation
[OH:1][C:2]1[CH:8]=[C:7]([C:9]([F:12])([F:11])[F:10])[CH:6]=[CH:5][C:3]=1[NH2:4].[C:13]1([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=2[N:25]=[C:26]=[O:27])[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>>[OH:1][C:2]1[CH:8]=[C:7]([C:9]([F:10])([F:11])[F:12])[CH:6]=[CH:5][C:3]=1[NH:4][C:26]([NH:25][C:20]1[CH:21]=[CH:22][CH:23]=[CH:24][C:19]=1[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)=[O:27]

Participants

3

Reactant 2

HCID 2222801-Isocyanato-2-phenylbenzeneHCID 155242772-Amino-5-(trifluoromethyl)phenol

Product 1

HCID 22011313N-(2-hydroxy-4-trifluoromethylphenyl) N'-(2-phenylphenyl)ureaYield 64%

Procedure

The urea was prepared from 2-hydroxy 4-trifluoromethyl aniline(example 7a, 0.171 g, 1 mmol)) and 2-phenylphenylisocyanate by general Method B. It was purified by dilution with methylene chloride and precipitation with hexane. Filtering afforded the desired compound(0.24 g, 64%). EI-MS m/z 373(M+H)+.

Workup

  1. customIt was purified by dilution with methylene chloride and precipitation with hexane
  2. filtrationFiltering

Sources & evidence

ORD record
ord-1386d8b51b45456d8c24c4c18e451577
Source dataset
uspto-grants-2001_01
Patent number
US06180675B2

Linked notes

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