2-Chloro-4-(ethylsulfonyl)-1-fluorobenzene → {3-Bromo-5-[2-chloro-4-(ethylsulfonyl)phenoxy]phenyl}acetic acid
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([CH2:9][C:10]([OH:12])=[O:11])[CH:5]=[C:6]([OH:8])[CH:7]=1.[CH2:13]([S:15]([C:18]1[CH:23]=[CH:22][C:21](F)=[C:20]([Cl:25])[CH:19]=1)(=[O:17])=[O:16])[CH3:14]>>[Br:1][C:2]1[CH:3]=[C:4]([CH2:9][C:10]([OH:12])=[O:11])[CH:5]=[C:6]([O:8][C:21]2[CH:22]=[CH:23][C:18]([S:15]([CH2:13][CH3:14])(=[O:17])=[O:16])=[CH:19][C:20]=2[Cl:25])[CH:7]=1Participants
3
Procedure
The title compound was prepared as described in example 2 step (iii) but instead using the product from step (v) and the product from example 3 step (i).
Sources & evidence
- ORD record
- ord-1893df8f72a542948c49bfc87ff9e937
- Source dataset
- uspto-grants-2012_04
- Patent number
- US08148572B2
Reaction notes
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