2-Aminophenol → HCID 68741489, compound

HRID 1969303

Reaction equation

HRID 1969303 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[OH:8].[Cl:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=1[C:16]1[O:20][C:19]([CH:21]=O)=[CH:18][CH:17]=1>>[Cl:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=1[C:16]1[O:20][C:19]([CH:21]=[N:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=2[OH:8])=[CH:18][CH:17]=1

Participants

3

Reactant 2

HCID 58012-AminophenolHCID 6098215-(2-Chlorophenyl)furfural

Product 1

HCID 68741489HCID 68741489, compound

Procedure

Using 2-aminophenol and 5-(2-chlorophenyl)furan-2-carbaldehyde, 2.69 g of 2-{[5-(2-chlorophenyl)furan-2-yl]methyleneamino}phenol were obtained as a yellow powder (yield 75%).

Sources & evidence

ORD record
ord-62a9241668a54d93b5f2dcb49217de94
Source dataset
uspto-grants-2013_04
Patent number
US08426540B2

Linked notes

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