2-Fluoro-5-(trifluoromethyl)benzaldehyde → [2-Bromo-5-(2-formyl-4-trifluoromethyl-phenoxy)-phenyl]-acetic acid methyl ester
Reaction equation
[CH3:1][O:2][C:3](=[O:13])[CH2:4][C:5]1[CH:10]=[C:9]([OH:11])[CH:8]=[CH:7][C:6]=1[Br:12].F[C:15]1[CH:22]=[CH:21][C:20]([C:23]([F:26])([F:25])[F:24])=[CH:19][C:16]=1[CH:17]=[O:18]>>[CH3:1][O:2][C:3](=[O:13])[CH2:4][C:5]1[CH:10]=[C:9]([O:11][C:15]2[CH:22]=[CH:21][C:20]([C:23]([F:26])([F:25])[F:24])=[CH:19][C:16]=2[CH:17]=[O:18])[CH:8]=[CH:7][C:6]=1[Br:12]Participants
3
Procedure
Prepared according to the procedure described in Example 9, Step 2, using the following starting materials: (2-bromo-5-hydroxy-phenyl)-acetic acid methyl ester and 2-fluoro-5-(trifluoromethyl)benzaldehyde.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-c8491212112542d7b9bd1262307db23e
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08242145B2
Reaction notes
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