2-Aminophenol → HCID 68777639, compound

HRID 1969302

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:11]=[C:12]([C:16]2[O:20][C:19]([CH:21]=O)=[CH:18][CH:17]=2)[CH:13]=[CH:14][CH:15]=1>>[Cl:9][C:10]1[CH:11]=[C:12]([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:13]=[CH:14][CH:15]=1

Participants

Reactant 2

HCID 58012-Aminophenol

HCID 6098225-(3-Chlorophenyl)furfural

Product 1

HCID 68777639HCID 68777639, compound

Procedure

Using 2-aminophenol and 5-(3-chlorophenyl)furan-2-carbaldehyde, 2.94 g of 2-{[5-(3-chlorophenyl)furan-2-yl]methyleneamino}phenol were obtained as a yellow powder (yield 82%).

Sources & evidence

ORD record: ord-91860d4c663f46ff917396ea8e66e86b
Source dataset: uspto-grants-2013_04
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08426540B2

Linked notes

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