Tert-Butylamine → 5'-((tert-Butylamino)methyl)-3,3''-dichloro-4,4''-bis(trifluoromethyl)-[1,1':3',1''-terphenyl]-4'-ol
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([C:12]2[CH:17]=[C:16]([CH:18]=O)[C:15]([OH:20])=[C:14]([C:21]3[CH:26]=[CH:25][C:24]([C:27]([F:30])([F:29])[F:28])=[C:23]([Cl:31])[CH:22]=3)[CH:13]=2)[CH:5]=[CH:6][C:7]=1[C:8]([F:11])([F:10])[F:9].[C:32]([NH2:36])([CH3:35])([CH3:34])[CH3:33]>>[C:32]([NH:36][CH2:18][C:16]1[C:15]([OH:20])=[C:14]([C:21]2[CH:26]=[CH:25][C:24]([C:27]([F:29])([F:28])[F:30])=[C:23]([Cl:31])[CH:22]=2)[CH:13]=[C:12]([C:4]2[CH:5]=[CH:6][C:7]([C:8]([F:11])([F:10])[F:9])=[C:2]([Cl:1])[CH:3]=2)[CH:17]=1)([CH3:35])([CH3:34])[CH3:33]Participants
3
Procedure
5′-((tert-Butylamino)methyl)-3,3″-dichloro-4,4″-bis(trifluoromethyl)-[1,1′:3′,1″-terphenyl]-4′-ol was prepared as a white solid using the procedure described in Example 5 from 3,3″-dichloro-4′-hydroxy-4,4″-bis(trifluoromethyl)-[1,1′:3′,1″-terphenyl]-5′-carbaldehyde and tert-butylamine.
Sources & evidence
- ORD record
- ord-ad3ecfddedbb46289f86241ddc587ffb
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09296696B2
Reaction notes
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