2-Aminophenol → HCID 867352, compound

HRID 1969304

Reaction equation

HRID 1969304 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][C:13]([C:16]2[O:20][C:19]([CH:21]=O)=[CH:18][CH:17]=2)=[CH:12][CH:11]=1>>[Cl:9][C:10]1[CH:11]=[CH:12][C:13]([C:16]2[O:20][C:19]([CH:21]=[N:1][C:2]3[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=3[OH:8])=[CH:18][CH:17]=2)=[CH:14][CH:15]=1

Participants

3

Reactant 2

HCID 58012-AminophenolHCID 6761845-(4-Chlorophenyl)-2-furaldehyde

Product 1

HCID 867352HCID 867352, compound

Procedure

Using 2-aminophenol and 5-(4-chlorophenyl)furan-2-carbaldehyde, 3.18 g of 2-{[5-(4-chlorophenyl)furan-2-yl]methyleneamino}phenol were obtained as a yellow powder (yield 89%).

Sources & evidence

ORD record
ord-ec5049e287774d189d6179d493b39cc1
Source dataset
uspto-grants-2013_04
Patent number
US08426540B2

Linked notes

Loading…