2-Amino-4-tert-butylphenol → HCID 68741389, compound

HRID 1969295Notes

Reaction equation

HRID 1969295 reaction equation
[NH2:1][C:2]1[CH:7]=[C:6]([C:8]([CH3:11])([CH3:10])[CH3:9])[CH:5]=[CH:4][C:3]=1[OH:12].[F:13][C:14]([F:29])([F:28])[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1[C:21]1[O:25][C:24]([CH:26]=O)=[CH:23][CH:22]=1>>[C:8]([C:6]1[CH:5]=[CH:4][C:3]([OH:12])=[C:2]([N:1]=[CH:26][C:24]2[O:25][C:21]([C:16]3[CH:17]=[CH:18][CH:19]=[CH:20][C:15]=3[C:14]([F:28])([F:13])[F:29])=[CH:22][CH:23]=2)[CH:7]=1)([CH3:9])([CH3:11])[CH3:10]

Participants

3

Reactant 2

HCID 709822-Amino-4-tert-butylphenolHCID 6882805-[2-(trifluoromethyl)phenyl]furan-2-carbaldehyde

Product 1

HCID 68741389HCID 68741389, compound

Procedure

Using 2-amino-4-tert-butylphenol and 5-(2-(trifluoromethyl)phenyl)furan-2-carbaldehyde, 4.25 g of 4-tert-butyl-2-{[5-(2-(trifluoromethyl)phenyl)furan-2-yl]methyleneamino}phenol were obtained as a yellow powder (yield 91%).

Sources & evidence

ORD record
ord-36c3718c90bd4f29885dc732fd7baf2d
Source dataset
uspto-grants-2013_04
Patent number
US08426540B2

Reaction notes

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