2-Aminophenol → HCID 68742675, compound

HRID 1969293Notes

Reaction equation

HRID 1969293 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[OH:8].[F:9][C:10]([F:25])([F:24])[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1[C:17]1[O:21][C:20]([CH:22]=O)=[CH:19][CH:18]=1>>[F:25][C:10]([F:9])([F:24])[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1[C:17]1[O:21][C:20]([CH:22]=[N:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=2[OH:8])=[CH:19][CH:18]=1

Participants

3

Reactant 2

HCID 58012-AminophenolHCID 6882805-[2-(trifluoromethyl)phenyl]furan-2-carbaldehyde

Product 1

HCID 68742675HCID 68742675, compound

Procedure

Using 2-Aminophenol and 5-(2-(trifluoromethyl)phenyl)furan-2-carbaldehyde, 3.53 g of 2-{[5-(2-(trifluoromethyl)phenyl)furan-2-yl]methyleneamino}phenol were obtained as a yellow powder (yield 89%).

Sources & evidence

ORD record
ord-5fe11fb887a84ae39e8ec5e297e3e7e6
Source dataset
uspto-grants-2013_04
Patent number
US08426540B2

Reaction notes

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