Ethyl 2-(4-bromophenyl)-2-methylpropanoate → 2-Methyl-2-(4-(5-(trifluoromethyl)pyridin-2-yl)phenyl)propanoic acid
Reaction equation
[CH3:1][C:2]([C:9]1[CH:14]=[CH:13][C:12]([C:15]2[CH:20]=[CH:19][C:18]([C:21]([F:24])([F:23])[F:22])=[CH:17][N:16]=2)=[CH:11][CH:10]=1)([CH3:8])[C:3]([O:5]CC)=[O:4].BrC1C=CC(C(C)(C)C(OCC)=O)=CC=1>>[CH3:8][C:2]([C:9]1[CH:10]=[CH:11][C:12]([C:15]2[CH:20]=[CH:19][C:18]([C:21]([F:23])([F:24])[F:22])=[CH:17][N:16]=2)=[CH:13][CH:14]=1)([CH3:1])[C:3]([OH:5])=[O:4]Participants
3
Procedure
The title compound was prepared according to the method of Example 22B, substituting the product of Example 26B for the product of Example 22A.
Sources & evidence
- ORD record
- ord-81e9553f70c2489badb6fa5e4900f9ca
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08993632B2
Reaction notes
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