4-(4-Bromo-2-chloro-phenoxy)-benzaldehyde-oxime → 4-(4-Bromo-2-trifluoromethyl-phenoxy)-benzaldehyde-oxime
Reaction equation
[Br:1][C:2]1[CH:17]=[CH:16][C:5]([O:6][C:7]2[CH:15]=[CH:14][C:10]([CH:11]=[N:12][OH:13])=[CH:9][CH:8]=2)=[C:4](Cl)[CH:3]=1.BrC1C=CC(OC2C=CC(C=O)=CC=2)=C([C:35]([F:38])([F:37])[F:36])C=1>>[Br:1][C:2]1[CH:17]=[CH:16][C:5]([O:6][C:7]2[CH:15]=[CH:14][C:10]([CH:11]=[N:12][OH:13])=[CH:9][CH:8]=2)=[C:4]([C:35]([F:38])([F:37])[F:36])[CH:3]=1Participants
3
Procedure
Prepared analogously to 78b) starting from 4-(4-bromo-2-trifluoromethyl-phenoxy)-benzaldehyde, it was further reacted directly without chromatographic purification.
Workup
- customwas further reacted directly without chromatographic purification
Sources & evidence
- ORD record
- ord-03df6480a4fc4a31b7a11c9f36adb73e
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08916589B2
Reaction notes
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