(3-Chloro-4-fluorophenyl)(phenyl)methanone → [3-(4-Benzoyl-2-chlorophenoxy)-5-(trifluoromethyl)phenyl]acetic acid
Reaction equation
[OH:1][C:2]1[CH:3]=[C:4]([CH2:12][C:13]([OH:15])=[O:14])[CH:5]=[C:6]([C:8]([F:11])([F:10])[F:9])[CH:7]=1.[Cl:16][C:17]1[CH:18]=[C:19]([C:24]([C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)=[O:25])[CH:20]=[CH:21][C:22]=1F>>[C:24]([C:19]1[CH:20]=[CH:21][C:22]([O:1][C:2]2[CH:3]=[C:4]([CH2:12][C:13]([OH:15])=[O:14])[CH:5]=[C:6]([C:8]([F:9])([F:10])[F:11])[CH:7]=2)=[C:17]([Cl:16])[CH:18]=1)(=[O:25])[C:26]1[CH:27]=[CH:28][CH:29]=[CH:30][CH:31]=1Participants
3
Procedure
The title compound was prepared as described in example 2 step (iii) but instead using the product from example 25 step (iv) and the product from step (i).
Sources & evidence
- ORD record
- ord-c15ffc05120943818e306b490d4fc8d5
- Source dataset
- uspto-grants-2012_04
- Patent number
- US08148572B2
Reaction notes
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