2-Aminophenol → 2-{[5-(4-Nitrophenyl)furan-2-yl]methyleneamino}phenol

HRID 1969300

Reaction equation

HRID 1969300 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[OH:8].[N+:9]([C:12]1[CH:17]=[CH:16][C:15]([C:18]2[O:22][C:21]([CH:23]=O)=[CH:20][CH:19]=2)=[CH:14][CH:13]=1)([O-:11])=[O:10]>>[N+:9]([C:12]1[CH:13]=[CH:14][C:15]([C:18]2[O:22][C:21]([CH:23]=[N:1][C:2]3[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=3[OH:8])=[CH:20][CH:19]=2)=[CH:16][CH:17]=1)([O-:11])=[O:10]

Participants

3

Reactant 2

HCID 58012-AminophenolHCID 815675-(4-Nitrophenyl)-2-furaldehyde

Product 1

HCID 46976362-{[5-(4-Nitrophenyl)furan-2-yl]methyleneamino}phenol

Procedure

Using 2-aminophenol and 5-(4-nitrophenyl)furan-2-carbaldehyde, 3.62 g of 2-{[5-(4-nitrophenyl)furan-2-yl]methyleneamino}phenol were obtained as a yellow powder (yield 98%).

Sources & evidence

ORD record
ord-c4a735c49e8b4cc3ae174d5827ea4229
Source dataset
uspto-grants-2013_04
Patent number
US08426540B2

Linked notes

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